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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398628Generated: October 29, 2026

Water → HCID 22315284, compound

https://huagongshe.com/reaction/398628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium HydroxideHCID 14923—
ReactantBoron tribromideHCID 25134—
ReactantHCID 22315143HCID 22315143—
SolventDichloromethaneHCID 6344—
ProductHCID 22315284HCID 2231528415.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

A 1.0M solution of boron tribromide in methylene chloride (7.43 mL, 7.43 mmol) at 25° C. was treated with a solution of 3-cyclopentyl-2-(3,4-dimethoxy-phenyl)-N-thiazol-2-yl-propionamide (prepared as in Example 113, 0.27 g, 0.74 mmol) in methylene chloride (7.43 mL). This solution was stirred at 25° C. for 1 h. At this time, the reaction was cooled to 0° C. and treated with a dilute aqueous ammonium hydroxide solution. This mixture was stirred at 0° C. for 20 min. At this time, the reaction was poured into water and was extracted with chloroform (3×50 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 70/30 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(3,4-dihydroxy-phenyl)-N-thiazol-2-yl-propionamide (38.8 mg, 15.7%) as a white solid: mp 170-173° C.; EI-HRMS m/e calcd for C17H20N2O3S (M+) 332.1194 found 332.1192.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610846B1
Source datasetuspto-grants-2003_08
ORD IDord-f9e8df0da98b4887a1cdd8c84af7c09d
Source noteuspto-grants-2003_08