戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 575158作成日:2026年10月25日

1-Methylpyrrolidine-2-methylamine → HCID 71715226、化合物

https://huagongshe.com/reaction/575158

反応式

関与物質

役割名称HCID仕込み量
反応物1-Methylpyrrolidine-2-methylamineHCID 117300—
反応物2-Carbamoyl-9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-3-carboxylic acidHCID 86693171—
生成物HCID 71715226HCID 71715226—

反応手順

2-Carbamoyl-9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-3-carboxylic acid (0.05 g) was reacted with (1-methylpyrrolidin-2-yl)methylamine similar to as described in Example 2 to afford 7.6 mg of (±) 9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-N3-[(1-methylpyrrolidin-2-yl)methyl]-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2,3-dicarboxamide following reverse phase hplc purification. MS (Q1) 470 (M)+. 1H NMR (400 MHz, DMSO) δ 8.58 (d, J=8.5 Hz, 1H), 7.74 (s, 1H), 7.27 (s, 1H), 7.01 (d, J=10.4, 4.6 Hz, 1H), 4.67-4.44 (m, 2H), 4.44-4.14 (m, 2H), 2.96 (s, 2H), 2.36 (s, 1H), 2.02-1.86 (m, 2H), 1.83 (s, 1H), 1.78-1.62 (m, 1H), 1.49 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09034866B2
出典データセットuspto-grants-2015_05
ORD IDord-2a008b2c60b04d3d9ca9f5bb66dd3ed8
出典メモuspto-grants-2015_05