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HRID 1676395作成日:2026年10月27日

1H-Benzimidazole-2-acetic acid → 2-(1H-benzo[d]imidazol-2-yl)-N-(3-fluoro-4-(2-(4-(morpholine-4-carbonyl)phenyl)thieno[3,2-b]pyridin-7-yloxy)phenyl)acetamide

https://huagongshe.com/reaction/1676395

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Benzimidazole-2-acetic acidHCID 26117—
反応物(4-(7-(4-Amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)phenyl)(morpholino)methanoneHCID 67347265—
生成物2-(1H-benzo[d]imidazol-2-yl)-N-(3-fluoro-4-(2-(4-(morpholine-4-carbonyl)phenyl)thieno[3,2-b]pyridin-7-yloxy)phenyl)acetamideHCID 589494926%

反応手順

Prepared from (4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)phenyl)(morpholino)methanone (Example 129, Step A) and 2-(1H-benzo[d]imidazol-2-yl)acetic acid according to the procedure of Example 89. The crude was purified by preparative HPLC to afford the desired product (1.9 mg, 6%). LRMS (ESI pos) m/e 607.9 (M+1). 1H-NMR (400 MHz, CD3OD) δ 8.53 (d, 1H), 7.94 (m, 4H), 7.81 (m, 2H), 7.61 (m, 4H), 7.47 (m, 2H), 6.74 (d, 1H), 3.73 (m, 8H), 3.50 (m, 2H); 19F NMR (376 MHz, CD3OD) δ −129.6.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08003662B2
出典データセットuspto-grants-2011_08
ORD IDord-2a21113bc3cc4e44aec64cb4eaaece3c
出典メモuspto-grants-2011_08