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HRID 468800作成日:2026年10月26日
Bromodifluoromethyl diethylphosphonate → N-(7-(Difluoromethoxy)isoquinolin-3-yl)cyclopropanecarboxamide
https://huagongshe.com/reaction/468800
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bromodifluoromethyl diethylphosphonate | HCID 144101 | — |
| 反応物 | N-(7-hydroxyisoquinolin-3-yl)cyclopropanecarboxamide | HCID 67975011 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | Acetonitrile--water (1/1) | HCID 18373917 | — |
| 生成物 | N-(7-(Difluoromethoxy)isoquinolin-3-yl)cyclopropanecarboxamide | HCID 67976733 | 38.5% |
反応手順
A solution of N-(7-hydroxyisoquinolin-3-yl)cyclopropanecarboxamide (91.2 mg, 0.40 mmol), diethyl bromodifluoromethylphosphonate (212 mg, 0.80 mmol) in acetonitrile/water (1:1, 5 mL) was mixed and stirred at −78° C. After the reaction mixture was warmed to room temperature and stirred for 20 minutes, the reaction mixture was diluted with ethyl acetate, and the organic phase was separated. The water phase was extracted with ethyl acetate, and the combined organic layer was dried, concentrated and purified by prep-HPLC to give product (42.8 mg, 26%). LCMS (ESI): RT (min)=0.994, M+H+=279.0, method=A. 1H NMR (400 MHz, DMSO-d6) δ 8.92 (s, 1H), 8.54 (s, 1H), 8.37 (s, 1H), 7.79 (d, J=8.8 Hz, 1H), 7.54 (s, 1H), 7.43 (dd, J=2.4, 8.8 Hz, 1H), 6.61 (t, J=73.2 Hz, 1H), 1.71-1.57 (m, 1H), 1.15-1.11 (m, 2H), 0.95-0.89 (m, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08623889B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-aef7cf60683146efa12c723ea2853134 |
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| 出典メモ | uspto-grants-2014_01 |
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