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HRID 496284作成日:2026年10月26日

Water → Phenyl 6-methoxypyridin-3-ylcarbamate

https://huagongshe.com/reaction/496284

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PyridineHCID 1049—
反応物Phenyl chloroformateHCID 15891—
反応物6-Methoxy-3-pyridinylamineHCID 81121—
溶媒DichloromethaneHCID 6344—
生成物Phenyl 6-methoxypyridin-3-ylcarbamateHCID 20185962—

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06943199B2
出典データセットuspto-grants-2005_09
ORD IDord-f8acd6879bec43138282c3654376f1d2
出典メモuspto-grants-2005_09