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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896568Generated: October 31, 2026

Pyridine → 4-Nitrophenyl benzo[d]thiazol-2-ylcarbamate

https://huagongshe.com/reaction/1896568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzo(d)thiazol-2-amineHCID 8706—
Reactant4-Nitrophenyl chloroformateHCID 82129—
SolventDichloromethaneHCID 6344—
Product4-Nitrophenyl benzo[d]thiazol-2-ylcarbamateHCID 5941867697.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

The title compound 4-nitrophenyl benzo[d]thiazol-2-ylcarbamate (19) was prepared by the following procedure: To 2-aminobenzothiazole (5.0 g, 30 mmol) was added DCM (36 mL) and the reaction mixture was stirred at 0° C. for 15 minutes. Then, p-nitrophenyl chloroformate (6.64 g, 33 mmol) in DCM (60 mL) was added, followed by pyridine (2.66 mL, 33 mmol) in DCM (36 mL). The reaction mixture was stirred and allowed to warm to rt overnight. The reaction mixture was filtered, washed with DCM, and dried to provide 9.22 g (90%) of the desired product 4-nitrophenyl benzo[d]thiazol-2-ylcarbamate (19): LC/MS (APCI): m/z 316.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518970B2
Source datasetuspto-grants-2013_08
ORD IDord-ed1c3f7e5bfe4ebba86fba58fa6ff3a4
Source noteuspto-grants-2013_08