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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280004Generated: October 30, 2026

Benzo(d)thiazol-2-amine → HCID 10180348, compound

https://huagongshe.com/reaction/1280004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(d)thiazol-2-amineHCID 8706—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-cyclopentyl-2-(3,4-dichlorophenyl)propanoic AcidHCID 2762725—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 10180348HCID 1018034842.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid (prepared as in Example 1, 0.133 g, 0.465 mmol) in methylene chloride (2.5 mL) cooled to 0° C. was treated with a 2M solution of oxalyl chloride in methylene chloride (0.3 mL, 1.0 mmol) and N,N-dimethylformamide (1 drop). The reaction mixture was stirred at 0° C. for 30 min and then treated with a solution of 2-aminobenzothiazole (0.087 g, 0.58 mmol) in methylene chloride (2.5 mL) followed by N,N-diisopropylethylamine (0.2 mL, 2.14 mmol). The reaction mixture was stirred at 25° C. for 16 h. The reaction mixture was then diluted with water (10 mL) and extracted with methylene chloride (3×10 mL). The combined organic layers were sequentially washed with water (1×10 mL), a 1N aqueous sodium hydroxide solution (1×10 mL), a 1N aqueous hydrochloric acid solution (1×10 mL), and a saturated aqueous sodium chloride solution (1×10 mL). The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 80/20 hexanes/ethyl acetate) afforded the N-benzothiazol-2-yl-3-cyclopentyl-2-(3,4-dichloro-phenyl)-propionamide (0.082 g, 42%) as a white solid: mp 104-105° C.; EI-HRMS m/e calcd for C21H20Cl2N2OS (M+) 418.0673, found 418.0674.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448399B1
Source datasetuspto-grants-2002_09
ORD IDord-53d42839a8454f02be279683fcc46a3d
Source noteuspto-grants-2002_09