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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzo(d)thiazol-2-amine | HCID 8706 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Nitrophenyl benzo[d]thiazol-2-ylcarbamate | HCID 59418676 | 97.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518970B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-ed1c3f7e5bfe4ebba86fba58fa6ff3a4 |
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| Source note | uspto-grants-2013_08 |
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