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HRID 1070419作成日:2026年10月26日

Diisopropylethylamine → HCID 10110214、化合物

https://huagongshe.com/reaction/1070419

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物3'-Methyl-biphenyl-4-carboxylic acidHCID 2759816—
反応物10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepineHCID 15547048—
溶媒DichloromethaneHCID 6344—
溶媒Thionyl ChlorideHCID 24386—
生成物HCID 10110214HCID 1011021482.9%

反応手順

A suspension of 3′-methyl-[1,1′-biphenyl]-4-carboxylic acid of Step B (0.50 g, 2.36 mmol) in thionyl chloride (3 mL) was heated at reflux for 30 minutes. After cooling, the thionyl chloride was removed in vacuo. The residue was dissolved in toluene and concentrated in vacuo to give the crude acid chloride as a yellow oil. The acid chloride was then dissolved in dichloromethane (5 mL) and slowly added to a solution of the 10,11-dihydro-5H-pyrrolo [2,1-c][1,4]benzodiazepine (0.65 g, 3.53 mmol) and N,N-diisopropylethyl amine (0.90 mL, 5.17 mmol) in dichloromethane (15 mL). After stirring for 2 hours, the reaction was quenched with water. The organic layer was washed with 1 N hydrochloric acid, 1 N sodium hydroxide and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo to give a white foam. Purification of the residue by flash chromatography using a solvent gradient from 15% to 25% of ethyl acetate in hexane gave a white foam which was crystallized by sonication from ethyl acetate/hexane to provide the title compound (0.74 g, 82.8%) as a white solid, m.p. 128-130° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06903091B2
出典データセットuspto-grants-2005_06
ORD IDord-441f3ddb4936485480806a2e57259a9f
出典メモuspto-grants-2005_06