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HRID 720118作成日:2026年10月25日

Triethylamine → (1r,2r)-2-Phenyl-cyclopropanecarboxylic acid [2-(3-dimethylaminomethyl-phenyl)-6-oxo-5,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl]-amide

https://huagongshe.com/reaction/720118

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物trans-2-Phenylcyclopropanecarboxylic acidHCID 237413—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物N-[2-(3-Dimethylaminomethyl-phenyl)-6-oxo-5,6-dihydro-1H-[1,21diazepino[4.5.6-cd]indol-8-yl]-2-fluoro-3-trifluoromethyl-benzamideHCID 135405075—
溶媒IsopropanolHCID 3776—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物(1r,2r)-2-Phenyl-cyclopropanecarboxylic acid [2-(3-dimethylaminomethyl-phenyl)-6-oxo-5,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl]-amideHCID 13614163076.1%

反応手順

Preparation of example 83a from Intermediate 73(d) of Example 73 (0.11 g, 0.33 mmol), (1R,2R)-2-phenyl-cyclopropanecarboxylic acid (0.08 g, 0.5 mmol), triethylamine (0.183 mL, 1.32 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.188 g, 0.5 mmol) and N,N-dimethylformamide (0.2 M, 1.7 mL) was carried out analogously to Example 11. Silica gel chromatography (90:10 to 80:20 CH2Cl2/2M ammonia in isopropyl alcohol) afforded the title compound (0.12 g) as powder in 76% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07132533B2
出典データセットuspto-grants-2006_11
ORD IDord-ce3e7ad7bb5d4bf8b80f530caaaa50d1
出典メモuspto-grants-2006_11