HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenyl chloroformate → 4-Nitrophenyl 2-methylbenzo[d]thiazol-5-ylcarbamate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | 2-Methylbenzothiazol-5-ylamine dihydrochloride | HCID 16218943 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-Nitrophenyl 2-methylbenzo[d]thiazol-5-ylcarbamate hydrochloride | HCID 66796936 | — |
Reaction Steps
5-Amino-2-methylbenzothiazole dihydrochloride (530 mg, 2.23 mmol) was dissolved in 1 N NaOH (10 mL) and was extracted with EtOAc (3×20 mL). The combined extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure. The material was dissolved in CH2Cl2 (10 mL), p-nitrophenyl chloroformate (586 mg, 2.91 mmol) was added, and the reaction mixture was stirred at rt overnight. The resulting solid was collected by filtration, was washed with CH2Cl2, and was dried under vacuum. This gave 853 mg of the title compound contaminated with some 5-amino-2-methylbenzothiazole. LC-MS: RT=8.49 min, [M+H]+=330.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428522B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-d6583dd6d5424dbfa291b5a82281002d |
| Source note | uspto-grants-2016_08 |