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HRID 6876作成日:2026年10月24日

Triethylsilane → N-cyclopropyl-2,4-difluoro-5-((2-(pyridin-2-ylamino)thiazol-5-yl)methylamino)benzamide

https://huagongshe.com/ja/reaction/6876

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylsilaneHCID 12052—
反応物5-amino-N-cyclopropyl-2,4-difluorobenzamideHCID 21966507—
反応物2-(Pyridin-2-ylamino)thiazole-5-carbaldehydeHCID 22019058—
溶媒Trifluoroacetic acid methylene chlorideHCID 21863450—
生成物N-cyclopropyl-2,4-difluoro-5-((2-(pyridin-2-ylamino)thiazol-5-yl)methylamino)benzamideHCID 1163273747.3%

反応手順

A mixture of 2-[pyridin-2-ylamino]-thiazole-5-carbaldehyde (41.0 mg, 0.2 mmol) and 5-amino-N-cyclopropyl-2,4-difluorobenzamide (46.6 mg, 0.22 mmol) in TFA/DCM (1:1, 1 mL) was stirred at RT for 10 min and triethylsilane (0.1 mL) was added. The mixture was stirred for 1 h, then concentrated and the residue was neutralized with NaHCO3 solution and the precipitates occurred. The precipitates were collected, washed with water and dried. The solid was triturated with MeOH and filtered to afford the title compound as a grayish solid (38 mg, 47%). Small amount of solid was boiled in methanol, the mixture was cooled to RT and filtered to afford a white solid. MS m/z 402 (M+H)+. 1H NMR (DMSO-d6) δ 8.23 (d, 1H, J=4.0 Hz), 8.15 (s, 1 H), 7.65 (t, 1 H, J=7.15 Hz), 7.26 (s, 1 H), 7.16 (m, 1 H), 7.01 (d, 1 H, J=8.75 Hz), 6.95 (m, 1 H), 6.89 (t, 1 H, J=7.15 Hz), 6.12 (s 1 H), 4.43 (m, 2 H), 2.79 (m, 1 H), 0.69 (m, 2 H), 0.51 (m, 2 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084160B2
出典データセットuspto-grants-2006_08
ORD IDord-c09aa937df8b486caaee08ce9bc04f1a
出典メモuspto-grants-2006_08