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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785477Generated: October 30, 2026

Water → 2-Benzoimidazol-1-yl-4-phenyl-thiazole-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1785477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzimidazoleHCID 5798—
ReactantEthyl 2-chloro-4-phenyl-1,3-thiazole-5-carboxylateHCID 13041816—
ReactantHCID 178418261HCID 178418261—
SolventTetrahydrofuranHCID 8028—
Product2-Benzoimidazol-1-yl-4-phenyl-thiazole-5-carboxylic acid ethyl esterHCID 5759584961.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-chloro-4-phenylthiazole-5-carboxylic acid ethyl ester (134 mg, 0.5 mmol), benzimidazole (Aldrich) (73.8 mg, 0.625 mmol) and LiN(TMS)2 (1N tetrahydrofuran solution, 0.63 ml) in tetrahydrofuran (2 ml) was heated in a micro-wave oven at 120° C. for 30 min. Water (3 ml) was added and the mixture was filtered, washed with water and ethyl acetate, dried in air flow to give 2-(benzoimidazol-1-yl)-4-phenylthiazole-5-carboxylic acid ethyl ester (108 mg, 61%). The aqueous solution was concentrated to remove tetrahydrofuran and then extracted with ethyl acetate to recover an additional amount of the product (100 mg, 75% pure). 1H-NMR (CDCl3) 8.84 (s, 1H); 8.16 (d, 1H); 7.81-7.90 (m, 3H); 7.39-7.58 (m, 5H); 4.37 (q, 2H); 1.27 (t, 3H). MS M/z 350 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504513B2
Source datasetuspto-grants-2009_03
ORD IDord-c9ff6485c25c4a798f1ff4bd86c8e00b
Source noteuspto-grants-2009_03