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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178219Generated: November 1, 2026

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

https://huagongshe.com/reaction/2178219

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 numberUS09067928B2
Source datasetuspto-grants-2015_06
ORD IDord-bea330e3788d4d42ad6aab41245691ac
Source noteuspto-grants-2015_06