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HRID 1179977作成日:2026年10月27日

6-methoxy-N-methylpyridin-2-amine → (6-Methoxy-pyridin-2-yl)-methyl-carbamic Acid 4-(5-trifluoromethyl-pyridin-2-yloxy)-phenyl Ester

https://huagongshe.com/reaction/1179977

反応式

関与物質

役割名称HCID仕込み量
反応物6-methoxy-N-methylpyridin-2-amineHCID 7019168—
反応物4-(5-Trifluoromethylpyridin-2-yloxy)-phenyl chloroformateHCID 22047762—
生成物(6-Methoxy-pyridin-2-yl)-methyl-carbamic Acid 4-(5-trifluoromethyl-pyridin-2-yloxy)-phenyl EsterHCID 69520765—

反応手順

The crude product was prepared from 4-(5-trifluoromethyl-pyridin-2-yloxy)-phenyl chloroformate and and 2-methoxy-6-methylaminopyridine. The reaction mixture was evaporated to dryness, dissolved in dichloromethane (100 ml) and extracted with a aqueous phosphate buffer, pH 7. The aqueous phase was extracted with dichloromethane (100 ml×2) and the combined organic phases were dried and evaporated to dryness. The product was subjected to flash chromatography, ethyl acetate/heptane (1:7) to give the titlew product (86%, white crystals). HPLC-MS m/z=420.4 (M+1), Rt: 5.23 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07279470B2
出典データセットuspto-grants-2007_10
ORD IDord-c3611bc78e9842a4b4f7bad494f4fb60
出典メモuspto-grants-2007_10