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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487732Generated: October 25, 2026

4-Nitrophenyl chloroformate → 4-Nitrophenyl 2-methylbenzo[d]thiazol-5-ylcarbamate hydrochloride

https://huagongshe.com/reaction/1487732

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant2-Methylbenzothiazol-5-ylamine dihydrochlorideHCID 16218943—
SolventSodium HydroxideHCID 14798—
Product4-Nitrophenyl 2-methylbenzo[d]thiazol-5-ylcarbamate hydrochlorideHCID 66796936—

Reaction Steps

5-Amino-2-methylbenzothiazole dihydrochloride (530 mg, 2.23 mmol) was dissolved in 1 N NaOH (10 mL) and was extracted with EtOAc (3×20 mL). The combined extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure. The material was dissolved in CH2Cl2 (10 mL), p-nitrophenyl chloroformate (586 mg, 2.91 mmol) was added, and the reaction mixture was stirred at rt overnight. The resulting solid was collected by filtration, was washed with CH2Cl2, and was dried under vacuum. This gave 853 mg of the title compound contaminated with some 5-amino-2-methylbenzothiazole. LC-MS: RT=8.49 min, [M+H]+=330.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428522B2
Source datasetuspto-grants-2016_08
ORD IDord-d6583dd6d5424dbfa291b5a82281002d
Source noteuspto-grants-2016_08