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HRID 1676834作成日:2026年10月27日

Sodium Carbonate → 4-(7,7-difluoro-9-isopropyl-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-N-(3-dimethylamino-propyl)-3-methoxy-benzamide

https://huagongshe.com/reaction/1676834

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物4-amino-N-[3-(dimethylamino)propyl]-3-methoxybenzamideHCID 58015058—
反応物2-Chloro-7,7-difluoro-9-isopropyl-5-methyl-5,7,8,9-tetrahydro-pyrimido[4,5-b][1,4]diazepin-6-oneHCID 86635900—
溶媒IsopropanolHCID 3776—
溶媒DichloromethaneHCID 6344—
生成物4-(7,7-difluoro-9-isopropyl-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-N-(3-dimethylamino-propyl)-3-methoxy-benzamideHCID 4454689153.6%

反応手順

A mixture of 0.07 g (0.24 mmole) of 2-chloro-7,7-difluoro-9-isopropyl-5-methyl-5,7,8,9-tetrahydro-pyrimido[4,5-b][1,4]diazepin-6-one (VII-292), 0.067 g (0.26 mmole) of 4-amino-N-(3-dimethylamino-propyl)-3-methoxy-benzamide, 0.069 g (0.36 mmole) of p-toluenesulfonic acid monohydrate and 4 mL of isopropanol was heated in a pressure tube at 140 degrees overnight. After cooling, dichloromethane and saturated sodium carbonate were added. The mixture was extracted with dichloromethane twice. The combined organic layers were washed three times with sodium carbonate, three times with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification by silica gel chromatography, eluting with dichloromethane-methanol (gradient, 100:0-0:100) gave 0.065 g of give 4-(7,7-difluoro-9-isopropyl-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-N-(3-dimethylamino-propyl)-3-methoxy-benzamide (I-296) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08003785B2
出典データセットuspto-grants-2011_08
ORD IDord-ce37a7b1739d4ac4996f809ece776b66
出典メモuspto-grants-2011_08