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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062989Generated: October 26, 2026

Pyridine → 5-Methyl-thiophene-2-carboxylic acid (4-chloro-benzothiazol-2-yl)-amide

https://huagongshe.com/reaction/1062989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Benzothiazolamine, 4-chloro-HCID 29872—
Reactant5-Methylthiophene-2-carbonyl chlorideHCID 2760083—
SolventDichloromethaneHCID 6344—
Product5-Methyl-thiophene-2-carboxylic acid (4-chloro-benzothiazol-2-yl)-amideHCID 86584916—

Reaction Steps

2-Amino-4-chlorobenzothiazol (92 mg, 0.50 mmol) is dissolved in dichloromethane (10 ml) and treated with pyridine (0.060 ml, 0.75 mmol) and 5-methyl-thiophene-2-carbonyl chloride (97 mg, 0.60 mmol). The reaction mixture is stirred at ambient temperature for 18 h and then evaporated to dryness. The residue is redissolved in ethyl acetate and water, the phases are separated and the organic layer extracted with brine. After dryin with sodium silfate, the solvent is removed in vacuo Flash chromatography on silica (eluent ethyl acetate/cyclohexane 1:4 affords the product as white solid.(88 mg, 57%). MS: m/e=308 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06963000B2
Source datasetuspto-grants-2005_11
ORD IDord-3f6db65703314a8cac3e708e206d598a
Source noteuspto-grants-2005_11