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HRID 587159作成日:2026年10月24日

2-Benzylpyrrolidine → 3-[(4-(2-Benzylpyrrolidin-1-yl)-1,3,5-triazin-2-yl)amino]-benzenemethanesulfonamide

https://huagongshe.com/ja/reaction/587159

反応式

関与物質

役割名称HCID仕込み量
反応物2-BenzylpyrrolidineHCID 339556—
反応物rac-3-[(4-(2-Methoxymethylpiperidin-1-yl)-1,3,5-triazin-2-yl)amino]-benzenemethanesulfonamideHCID 60197106—
反応物3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamideHCID 86679822—
生成物3-[(4-(2-Benzylpyrrolidin-1-yl)-1,3,5-triazin-2-yl)amino]-benzenemethanesulfonamideHCID 60197407—

反応手順

B26 was prepared following the procedure reported for B4 using A1 and rac-2-benzylpyrrolidine. It was obtained as a white crystalline solid; yield: 160 mg (42%). 1H NMR (300 MHz, d6-DMSO, 300K) δ 1.67-1.92 (m, 4H), 2.57-2.77 (m, 1H), 3.03-3.21 (m, 1H), 3.42-3.62 (m, 2H), 4.20 (2 s, 2H), 4.28-4.48 (m, 1H), 6.88 (bs, 2H), 6.93-7.08 (m, 1H), 7.12-7.38 (m, 6H), 7.58 and 7.71 (2 m, 1H), 7.82-8.01 (m, 1H), 8.23 and 8.30 (2 s, 1H), 9.66 (bs, 1H). MS (ES) C21H24N6O2S requires: 424. found: 425 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09226929B2
出典データセットuspto-grants-2016_01
ORD IDord-19706696b23d4ebaaa621b9c708286c8
出典メモuspto-grants-2016_01