The development and application of a novel trideuterium methylation reagent
Source abstract
Abstract
The incorporation of a trideuteromethyl group in diverse pharmaceutical building blocks and drug-like molecules serves as a valuable strategy in medicinal and industrial chemistry. Trideuteromethylation reactions have gained significant, continuous attention at a rapid pace in recent years. However, the lack of known trideuteromethylated reagents prevents the range of applications in terms of substrate and reaction type. In this study, we report the synthesis and application of trideuteromethyl thianthrenium triflate (TT-CD3+OTf−) as a trideuteromethylating reagent that makes use of inexpensive raw material. This reagent performs well in nucleophilic, radical, and transition-metal-catalyzed C–H trideuteromethylations. Microflow technique can enhance and intensify these processes resulting in various trideuteromethylated organic molecules and deuterated pharmaceuticals with comparable yields and high deuterium content.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Chemical Reactions and Isotopes · Epigenetics and DNA Methylation
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (81)
Show source-provided references
1. The methylation effect in medicinal chemistry10.1021/cr200060g ↗
2. Profound methyl effects in drugs discovery and a Call for new C-H methylation reactions10.1002/anie.201303207 ↗
3. Insights into the impact of N- and O- methylation on aqueous solubility and lipophilicity using matched molecular pair analysis10.1039/C5MD00309A ↗
4. The Importance of being Me: magic methyls, methyltransferase inhibitors, and the discovery of tazemetostat10.1021/acs.jmedchem.5b01501 ↗
5. Methyl effects on protein-ligand binding10.1021/jm3003697 ↗
6. Biphenyl amide p38 kinase inhibitors 3: improvement of cellular and in vivo activity10.1016/j.bmcl.2008.06.048 ↗
7. Using deuterium in drug discovery: leaving the label in the drug10.1021/jm4007998 ↗
8. Secondary kinetic isotope effects involving deuterated nucleophiles10.1039/cs9952400223 ↗
9. A potent and selective S1P1 Antagonist with efficacy in experimental autoimmune encephalomyelitis10.1016/j.chembiol.2012.07.016 ↗
10. Rational design of orthogonal receptor-ligand combinations10.1002/anie.199521291 ↗
11. Recent progress in methyl-radical-mediated methylation or demethylation reactions10.1021/acscatal.1c02010 ↗
12. Cobalt-catalysed C-H methylation for late-stage drug diversification10.1038/s41557-020-0475-7 ↗
13. Late-stage oxidative C(sp3)-H methylation10.1038/s41586-020-2137-8 ↗
14. Palladium-catalyzed methylation of aryl, heteroaryl, and vinyl boronate esters10.1021/acs.orglett.9b00025 ↗
15. Deuterium- and tritium-labelled compounds: applications in the life science10.1002/anie.201704146 ↗
16. On the interpretation of deuterium kinetic isotope effects in C-H bond functionalizations by transition-metal complexes10.1002/anie.201107334 ↗
17. Synthesis of 9-CD3-9-cis-retinal cofactor of isorhodopsin10.1016/j.tetlet.2018.11.034 ↗
18. Stable isotope compounds – production, detection, and application10.1016/j.biotechadv.2018.01.010 ↗
19. Deuterated drugs draw heavier backing10.1038/nrd.2016.63 ↗
20. Broadening of horizons in the synthesis of CD3-labeled molecules10.1039/D1CS00544H ↗
21. Applications of deuterium in medicinal chemistry10.1021/acs.jmedchem.8b01808 ↗
22. Deuterated drug molecules: focus on FDA-approved deutetrabenazine10.1021/acs.biochem.7b00765 ↗
23. Novel process for preparation of tetrabenazine and deutetrabenazine10.1021/acs.oprd.8b00011 ↗
24. Radical trideuteromethylation with deuterated dimethyl sulfoxide in the synthesis of heterocycles and labelled building blocks10.1039/C6CC07196A ↗
25. Iron-mediated azidomethylation or azidotrideuteromethylation of active alkenes with azidotrimethylsilane and dimethyl sulfoxide10.1002/adsc.201800078 ↗
26. Trideuteromethylation enabled by a sulfoxonium metathesis reaction10.1021/acs.orglett.8b03641 ↗
27. High resolution 1H detected 1H, 13C correlation spectra in MAS solid-state NMR using deuterated proteins with selective 1H, 2H isotopic labeling of methyl groups10.1021/ja064379m ↗
28. Use of radiolabeled compounds in drug metabolism and pharmacokinetic studies10.1021/tx2005212 ↗
29. The use of deuterium isotope effects to probe the active site properties, mechanism of cytochrome P450-catalyzed reactions, and mechanisms of metabolically dependent toxicity10.1124/dmd.31.12.1481 ↗
30. Synthesis of 19-trideuterated ent-testosterone and the GABAA receptor potentiators ent-androsterone and ent-etiocholanolone10.1002/jlcr.1558 ↗
31. Trideuteromethylation in dimethyl sulphoxide10.1016/S0040-4039(01)98967-1 ↗
32. C-H methylation of heteroarenes inspired by radical SAM methyl transferase10.1021/ja5007838 ↗
33. Synthesis of [N-trideuteromethyl] labelled E-doxepin10.1002/jlcr.2580330210 ↗
34. The application of dimethyl sulfoxide as reagent in organic synthesis10.1002/adsc.201501007 ↗
35. A general method for N-methylation of amines and nitro compounds with dimethylsulfoxide10.1002/chem.201303802 ↗
36. DNA methylation by dimethyl sulfoxide and methionine sulfoxide triggered by hydroxyl radical and implications for epigenetic modifications10.1016/j.bmcl.2009.10.124 ↗
37. Iron-catalysed tritiation of pharmaceuticals10.1038/nature16464 ↗
38. Palladium(II)-mediated C-H tritiation of complex pharmaceuticals10.1002/anie.201711364 ↗
39. Photoredox-catalyzed deuteration and tritiation of pharmaceutical compounds10.1126/science.aap9674 ↗
40. A general strategy for site-selective incorporation of deuterium and tritium into pyridines, diazines, and pharmaceuticals10.1021/jacs.7b11710 ↗
41. Stereoretentive deuteration of α-chiral amines with D2O10.1021/jacs.6b07879 ↗
42. General and practical potassium methoxide/disilane-mediated dehalogenative deuteration of (hetero)arylhalides10.1021/jacs.8b07597 ↗
43. Radical deuteration with D2O: catalysis and mechanistic insights10.1021/jacs.7b12105 ↗
44. Nickel-catalyzed deoxygenative deuteration of aryl sulfamates10.1002/adsc.201601105 ↗
45. Highly selective directed iridium-catalyzed hydrogen isotope exchange reactions of aliphatic amides10.1002/anie.201804010 ↗
46. Ruthenium-catalyzed hydrogen isotope exchange of C(sp3)-H bonds directed by a sulfur atom10.1039/C8CC00653A ↗
47. Regioselective deuteration of alcohols in D2O catalysed by homogenous manganese and iron pincer complexes10.1039/C8GC01052H ↗
48. Palladium-catalyzed regioselective C-H functionalization of arenes substituted by two N-heterocycles and application in late-stage functionalization10.1021/acs.joc.8b00322 ↗
49. Palladium-catalyzed H/D exchange reaction with 8-aminoquinoline as the directing group: access to ortho-selective deuterated aromatic acids and β-selective deuterated aliphatic acids10.1021/acs.joc.8b00734 ↗
50. Reductive deuteration of nitriles: the synthesis of α,α-dideuterio amines by sodium-mediated electron transfer reactions10.1021/acs.joc.8b01730 ↗
51. Controllable deuteration of halogenated compounds by photocatalytic D2O splitting10.1038/s41467-017-02551-8 ↗
52. One-pot synthesis of deuterated aldehydes from arylmethyl halides10.1021/acs.orglett.8b00016 ↗
53. Deoxygenative deuteration of carboxylic acids with D2O10.1002/anie.201811522 ↗
54. Trideutermethylation enabled by a sulfoxonium metathesis reaction10.1021/acs.orglett.8b03641 ↗
55. Bioinspired design of a robust d3-methylating agent
56. Green synthesis of α-deuterated boronates using DMTT reagent10.1016/j.gresc.2021.05.001 ↗
57. Site-selective and versatile aromatic C-H functionalization by thianthrenation10.1038/s41586-019-0982-0 ↗
58. Aryl sulfonium salts for site-selective late-stage trifluoromethylation10.1002/anie.201906672 ↗
59. C-N cross-couplings for site-selective late-stage diversification via aryl sulfonium salts10.1021/jacs.9b07323 ↗
60. Site-selective C-H oxygenation via aryl sulfonium salts10.1002/anie.201908718 ↗
61. Para-selective borylation of monosubstituted benzenes using a transient mediator10.1007/s11426-019-9652-x ↗
62. Photoredox catalysis with aryl sulfonium salts enables site-selective late-stage fluorination10.1038/s41557-019-0353-3 ↗
63. Allylic amination of alkenes with iminothianthrenes to afford alkyl allylamines10.1021/jacs.0c08248 ↗
64. Regioand stereoselective thianthrenation of olefins to access versatile alkenyl electrophiles10.1002/anie.201914215 ↗
65. Site-selective C-H functionalization-sulfination sequence to access aryl sulfonamides10.1021/acs.orglett.0c00982 ↗
66. Cine-substitutions at five-membered hetarenes enabled by sulfonium salts10.1021/acs.orglett.0c02067 ↗
67. Photoinduced copper-catalyzed site-selective C(sp2)-C(sp) cross-coupling via aryl sulfonium salts10.1021/acs.orglett.0c02364 ↗
68. Arylation of aryllithiums with S-arylphenothiazinium ions for biaryl synthesis10.1039/D0CC05830K ↗
69. Thianthrenation-enabled alpha-arylation of carbonyl compounds with arenes10.1021/acs.orglett.0c02913 ↗
70. End-to-end continuous flow synthesis and purification of diphenhydramine hydrochloride featuring atom economy, in-line separation, and flow of molten ammonium salts10.1039/c3sc50859e ↗
71. A three-minute synthesis and purification of ibuprofen: pushing the limits of continuous-flow processing10.1002/anie.201409093 ↗
72. A unified continuous flow assembly-line synthesis of highly substituted pyrazoles and pyrazolines10.1002/anie.201704529 ↗
73. A rapid total synthesis of ciprofloxacin hydrochloride in continuous flow10.1002/anie.201703812 ↗
74. Synthesis and utilization of nitroalkyne equivalents in batch and continuous flow10.1002/anie.201706157 ↗
75. Photoredox activation of carbon dioxide for amino acid synthesis in continuous flow10.1038/nchem.2690 ↗
76. Direct β-selective hydrocarboxylation of styrenes with CO2 enabled by continuous flow photoredox catalysis10.1021/jacs.7b05942 ↗
77. Modular continuous flow synthesis of imatinib and analogues10.1021/acs.orglett.9b02259 ↗
78. Green and sustainable chemical synthesis using flow microreactors10.1002/cssc.201000271 ↗
79. Continuous flow reactors: a perspective10.1039/C1GC16022B ↗
80. Synthesis of annulated pyridines by intramolecular inverse-electron-demand hetero-Diels-Alder reaction under superheated continuous flow conditions10.1002/ejoc.201101538 ↗
81. Chemical protein modification through cysteine10.1002/cbic.201500667 ↗