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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641056Generated: November 2, 2026

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

https://huagongshe.com/reaction/1641056

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 numberUS08114893B2
Source datasetuspto-grants-2012_02
ORD IDord-8e16dd7350b642cd8254dbb4aa61261a
Source noteuspto-grants-2012_02