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HRID 1420013作成日:2026年10月24日

Triethylamine → 9,10-Dihydro-10-(4-nitrobenzoyl)-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepine

https://huagongshe.com/ja/reaction/1420013

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Nitrobenzoyl chlorideHCID 8502—
反応物9,10-dihydro-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepineHCID 21837159—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物9,10-Dihydro-10-(4-nitrobenzoyl)-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepineHCID 21837151—

反応手順

To a solution of 10 mmol of 9,10-dihydro-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepine in 50 ml of methylene chloride under argon is added 15 mmol of triethylamine followed by ice bath cooling. A solution of 11 mmol of 4-nitrobenzoyl chloride in 10 ml of methylene chloride is added dropwise. Following complete addition, the ice bath is removed and the reaction mixture stirred at room temperature for 2 hours. The volatiles are removed in vacuo to give a residue which is dissolved in ethyl acetate. The solution is washed with water, 1N HCl, NaHCO3, and brine. The organic layer is dried with Na2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography on silica gel to give desired product as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05889001
出典データセットuspto-grants-1999_03
ORD IDord-87c86ea69c954bf093b95f0a0f119d54
出典メモuspto-grants-1999_03