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HRID 30413作成日:2026年10月24日

1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine → 4-[4-Fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ja/reaction/30413

反応式

関与物質

役割名称HCID仕込み量
反応物1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
反応物BEMP resinHCID 16216994—
反応物4-[1-(4-chloro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl esterHCID 68530176—
反応物HCID 178518865HCID 178518865—
溶媒DimethylformamideHCID 6228—
生成物4-[4-Fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl esterHCID 6853283651%

反応手順

4-[4-Fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 46) was prepared as described above for Intermediate 42 using Intermediate 45 (300 mg, 1.218 mmol), PS-BEMP resin (1.108 g) and 4-methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 2) (374 mg, 1.34 mmol) in DMF (10 ml) to afford 265 mg (51%) of Intermediate 46 as a yellow oil. MS (M+1)=430.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423054B2
出典データセットuspto-grants-2008_09
ORD IDord-150fdb8a77df4999909115a7edd9ba62
出典メモuspto-grants-2008_09