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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85117Generated: October 26, 2026

2-Aminothiazole → tert-butyl 3-(2-(4-(thiazol-2-ylcarbamoyl)-1H-benzo[d]imidazol-2-yl)phenoxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/85117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-(2-(1-(tert-butoxycarbonyl)pyrrolidin-3-yloxy)phenyl)-1H-benzo[d]imidazole-4-carboxylic acidHCID 67201505—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-butyl 3-(2-(4-(thiazol-2-ylcarbamoyl)-1H-benzo[d]imidazol-2-yl)phenoxy)pyrrolidine-1-carboxylateHCID 8665379048%

Reaction Steps

To a solution of 2-(2-(1-(tert-butoxycarbonyl)pyrrolidin-3-yloxy)phenyl)-1H-benzo[d]imidazole-4-carboxylic acid (31; 150 mg, 0.36 mmol), thiazol-2-amine (4; 35.5 mg, 0.36 mmol), and HATU (202 mg, 0.53 mmol) in DMF (5 mL) was added DIEA (137 mg, 1.06 mmol). The mixture was stirred at room temperature for 18 h. It was then diluted with water (20 mL) and stirred for 30 min. The precipitate was collected by filtration, and then purified by column chromatography to give 85 mg of the title compound 32 (yield: 48%). MS (ESI) calcd for C26H27N5O4S: 505.18; found: 506 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846947B2
Source datasetuspto-grants-2014_09
ORD IDord-989dc590c2ba425ea577f04c9b5db245
Source noteuspto-grants-2014_09