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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447148Generated: October 29, 2026

Water → Tert-butyl 2-(6-(3,4-dimethoxyphenylcarbamoyl)benzo[d]thiazol-2-ylamino)ethyl(methyl)carbamate

https://huagongshe.com/reaction/447148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-Boc-N-methylethylenediamineHCID 2756424—
Reactant2-bromo-N-(3,4-dimethoxyphenyl)benzo[d]thiazole-6-carboxamideHCID 67236223—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductTert-butyl 2-(6-(3,4-dimethoxyphenylcarbamoyl)benzo[d]thiazol-2-ylamino)ethyl(methyl)carbamateHCID 86654768—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-bromo-N-(3,4-dimethoxyphenyl)benzo[d]thiazole-6-carboxamide (392.4 mg, 0.998 mmol), N-(2-aminoethyl)-N-methyl carbamic acid tert-butyl ester (193.4 mg, 1.11 mmol) and N—N-diisopropylethylamine (148.6 mg, 1.15 mmol) in 1-methyl-2-pyrrolidinone (3 mL) was stirred in a preheated oil bath at 120° C. for 4 h, then allowed to cool to room temperature, poured into water and extracted into ethyl acetate. The organic layer was washed with water, dried (sodium sulfate), filtered and concentrated in vacuo. The resulting residue was purified by gradient flash column chromatography, eluting with 70% to 80% ethyl acetate in heptane to yield tert-butyl 2-(6-(3,4-dimethoxyphenylcarbamoyl)benzo[d]thiazol-2-ylamino)ethyl(methyl)carbamate as a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481547B2
Source datasetuspto-grants-2013_07
ORD IDord-5698f1c17520494aa0a74cbbb5156a8c
Source noteuspto-grants-2013_07