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HRID 1367970作成日:2026年10月25日

Diisopropylethylamine → HCID 178488012、化合物

https://huagongshe.com/reaction/1367970

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-Methylsulfonylbenzylamine hydrochlorideHCID 2729269—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
反応物2-[(isoquinoline-3-carbonyl)-amino]-5-methoxy-1H-benzoimidazole-4-carboxylic acidHCID 66940762—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物HCID 178488012HCID 17848801247.2%

反応手順

33 mg (0.1 mmol) of 2-[(isoquinoline-3-carbonyl)-amino]-5-methoxy-1H-benzoimidazole-4-carboxylic acid and 100 mg (0.25 mmol) of HBTU were dissolved in 1.0 mL of DMF and 0.4 mL of DIEA was treated with 32 mg (0.15 mmol) of 4-methanesulfonyl-benzylamine hydrochloride as described in general procedure A. Upon completion, the reaction was diluted with brine. The resulting solid was filtered, washed with water and EtOAc, and dried under vacuum to produce 25 mg (47%) of isoquinoline-3-carboxylic acid [7-(4-methanesulfonyl-benzylcarbamoyl)-6-methoxy-1H-benzoimidazol-2-yl]-amide. LCMS: 530 (M+1)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893267B2
出典データセットuspto-grants-2011_02
ORD IDord-4bea3aca54084f6caf90d171b1a8b426
出典メモuspto-grants-2011_02