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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250722Generated: October 26, 2026

Benzyl chloroformate → (4-Methoxy-7-phenyl-benzothiazol-2-yl)-carbamic acid benzyl ester

https://huagongshe.com/reaction/2250722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant2-Amino-4-methoxy-7-phenyl-benzothiazoleHCID 22283026—
SolventPyridineHCID 1049—
Product(4-Methoxy-7-phenyl-benzothiazol-2-yl)-carbamic acid benzyl esterHCID 8658492679.4%

Reaction Steps

To a stirred solution of 2-amino-4-methoxy-7-phenyl-benzothiazole (512 mg, 2 mmol) in pyridine at 90° C. was added benzyl chloroformate (3.3 ml, 23.4 mmol) in three portions over 6 hours. The reaction mixture was then evaporated to dryness and partioned between CH2Cl2 (50 ml) and saturated aqueous NaCl solution (50 ml), the aqueous phase was separated and extracted further with CH2Cl2 (2×50 ml) and the combined organic phases dried, filtered and evaporated. The crude residue was then chromatographed over SiO2 (Merck 230-400 mesh) eluting with CH2Cl2EtOAc (4:1) to afford the title compound as a white foam (620 mg, 79% yield), MS: m/e=391.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317007B2
Source datasetuspto-grants-2008_01
ORD IDord-e5023c21862d4ad2aa0941c23b2ad6c9
Source noteuspto-grants-2008_01