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HRID 1789491作成日:2026年10月27日

Ethanol → 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine

https://huagongshe.com/reaction/1789491

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Carbon TetrachlorideHCID 5943—
反応物BromineHCID 24408—
反応物N-[(1-acetyl-4-piperidinyl)methyl]-N'-phenylthioureaHCID 14048941—
溶媒AcetonitrileHCID 6342—
生成物1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamineHCID 14048944—

反応手順

To a stirred mixture of 5.8 parts of N-[(1-acetyl-4-piperidinyl)methyl]-N'-phenylthiourea and 160 parts of tetrachloromethane were added 3.7 parts of bromine. The whole was stirred and refluxed for 15 minutes. After the additions of 16 parts of ethanol and 16 parts of acetonitrile, the reaction mixture was cooled. The precipitated product was filtered off, washed with acetonitrile and dried. The hydrobromide salt was dissolved in methanol and water. This solution was alkalized with ammonium hydroxide. The precipitated product was filtered off, washed with water and dried, yielding 2.7 parts of 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine; mp. 138.1° C. (intermediate 29).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04689330
出典データセットuspto-grants-1987_08
ORD IDord-ee56261ae4364f3eb952ade8c36ca8dd
出典メモuspto-grants-1987_08