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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410742Generated: October 25, 2026

1,1'-Thiocarbonyldiimidazole → 1-Methyl-2-(6-trifluoromethyl-benzothiazol-2-ylamino)-1H-benzoimidazole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/410742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
Reactant2-Amino-6-(trifluoromethyl)benzothiazoleHCID 2735955—
ReactantMethyl 3-amino-4-(methylamino)benzoateHCID 15586064—
Solvent1,2-DichloroethaneHCID 11—
Product1-Methyl-2-(6-trifluoromethyl-benzothiazol-2-ylamino)-1H-benzoimidazole-5-carboxylic acid methyl esterHCID 5839767841.1%

Reaction Steps

1-Methyl-2-(6-trifluoromethyl-benzothiazol-2-ylamino)-1H-benzoimidazole-5-carboxylic acid methyl ester (765 mg) was prepared by following General Procedure D starting from 3-amino-4-methylamino-benzoic acid methyl ester (991 mg), 2-amino-6-(trifluoromethyl)benzothiazole (1.0 g), 1,1′-thiocarbonyldiimidazole (1.09 g), and EDC (1.32 g). LC/MS: m/z 407.9. 1H NMR (DMSO-d6, 400 MHz): δ 12.37 (bs, 1H), 8.15 (s, 1H), 7.97 (d, 1H), 7.95 (d, 1H), 7.85 (d, 1H), 7.62-7.43 (m, 2H), 3.86 (s, 3H), 3.62 (bs, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759535B2
Source datasetuspto-grants-2014_06
ORD IDord-8794ca0dfbb84ec39ee64180237b0611
Source noteuspto-grants-2014_06