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HRID 51149作成日:2026年10月24日

2-(Methylsulfonyl)ethanamine → N-{3-fluoro-4-[(3-fluorobenzyl)oxy]phenyl}-6-[5-({[2-(methanesulphonyl)ethyl]amino}methyl)-2-furyl]-4-quinazolinamine

https://huagongshe.com/ja/reaction/51149

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Methylsulfonyl)ethanamineHCID 4340561—
反応物5-(4-{3-Fluoro-4-(3-fluorobenzyloxy)anilino}-6-quinazolinyl)-furan-2-carbaldehydeHCID 21952282—
生成物N-{3-fluoro-4-[(3-fluorobenzyl)oxy]phenyl}-6-[5-({[2-(methanesulphonyl)ethyl]amino}methyl)-2-furyl]-4-quinazolinamineHCID 9915923—

反応手順

Prepared according to Procedure D from 5-(4-{3-fluoro-4-(3-fluorobenzyloxy)anilino}-6-quinazolinyl)-furan-2-carbaldehyde (0.6 equiv) and 2-methanesulphonyl-ethylamine (1 equiv). 1H NMR 400 MHz (DMSO-d6) 9.61 (bs, 2H); 9.28 (bs, 1H); 8.80 (s, 1H); 8.34 (d, 1H); 7.87 (m, 2H); 7.59 (d, 1H); 7.44 (m, 1H); 7.2-7.38 (m, 4H); 7.18 (m, 1H); 6.83 (s, 1H); 5.25 (s, 2H); 4.42 (s, 2H); 3.60 (m, 2H); 3.45 (m, 2H, obscured by water peak); 3.16 (s, 3H); MS m/z 565 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713485B2
出典データセットuspto-grants-2004_03
ORD IDord-d415ac3bacdd4e74a874e786a2e63b23
出典メモuspto-grants-2004_03