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HRID 47351作成日:2026年10月23日

Propyl isocyanate → 4-[2-[4-(3-Bromo-8-chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-piperazinyl]-2-oxoethyl]-N-propyl-1-piperidinecarboxamide

https://huagongshe.com/ja/reaction/47351

反応式

関与物質

役割名称HCID仕込み量
反応物Propyl isocyanateHCID 61033—
反応物1-(3-Bromo-8-chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-4-[(4-piperidinyl)acetyl]piperazineHCID 10768220—
溶媒DichloromethaneHCID 6344—
生成物4-[2-[4-(3-Bromo-8-chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-piperazinyl]-2-oxoethyl]-N-propyl-1-piperidinecarboxamideHCID 10769930112.9%

反応条件

温度25 °C

反応手順

1-(3-Bromo-8-chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-4-[(4-piperidinyl)acetyl]piperazine (Preparative Example 10) (490 mg, 0.8 mmoles) was dissolved in anhydrous dichloromethane (5 ml) and n-propyl isocyanate (322.1 mg, 3.2 mmoles) was added. The mixture was stirred under argon at 25° C. for 44 h. The solution was chromatographed on silica gel using 2% (10% concentrated NH4OH in methanol)dichloromethane as the eluant to give 544.8 mg of the title compound (Yield: 95%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699872B2
出典データセットuspto-grants-2004_03
ORD IDord-1951beaeb4f14e549384a1c72b7a7480
出典メモuspto-grants-2004_03