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HRID 720101作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/720101

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8-Amino-2-phenyl-1,5-dihydro-[1,2]diazepino[4,5,6-cd]indol-6-oneHCID 135774079—
溶媒DimethylformamideHCID 6228—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
溶媒Diethylether ethylacetateHCID 21584169—
生成物(1s,2s)-2-Phenyl-cyclopropanecarboxylic acid (6-oxo-2-phenyl-5,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)-amideHCID 13614166814%

反応手順

Preparation of example 45 from the title compound of Example 7 (30 mg, 0.11 mmol), ±trans-2-phenyl-1-cyclopropanecarboxylic acid (26 mg, 0.16 mmol), triethylamine (0.076 mL, 0.55 mmol), and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (62 mg, 0.16 mmol) in N,N-dimethylformamide (1.0 mL) was carried out analogously to Example 11. Silica gel chromatography (1:1 ethyl acetate:hexane), also in an analogous manner, followed by trituration with ethyl acetate/diethyl ether afforded the title compound (6.5 mg, 0.015 mmol) (mixture of trans diastereomers) as a yellow powder in 14% 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-aafa03db135d4e7798a69e9d008c23fd
出典メモuspto-grants-2006_11