HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Phenyl 6-methoxypyridin-3-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 6-Methoxy-3-pyridinylamine | HCID 81121 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenyl 6-methoxypyridin-3-ylcarbamate | HCID 20185962 | — |
Reaction Steps
6-Methoxy-pyridin-3-ylamine (1.0 g, 8.06 mmol) and pyridine (18 ml) are stirred in dry CH2Cl2. To this mixture phenylchloroformate (1.9 g, 12.0 mmol) is added and stirred for 24 hours at room temperature. Water and a solution of 1:1 EtOAc/hexanes is added to the mixture and the organic layer is separated. The organic layer is washed with 1N HCl three times and with brine once. The organic layer is dried over Na2SO4, filtered, and evaporated in vacuo. Purify by flash column chromatography (0-10% EtOAc/CH2Cl2) to obtain (6-methoxy-pyridin-3-yl)-carbamic acid phenyl ester. Mass spec.: m+1=245 (AP+). B. 1′-(6-methoxy-pyridin-3-yl-carbamoyl)-spiroisobenzofuran-1,4′-piperidine
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943199B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-f8acd6879bec43138282c3654376f1d2 |
| Source note | uspto-grants-2005_09 |