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HRID 575334作成日:2026年10月25日

(R)-2-(5-methyl-1,2,4-oxadiazol-3-yl)but-3-yn-2-ol → HCID 178422861、化合物

https://huagongshe.com/reaction/575334

反応式

関与物質

役割名称HCID仕込み量
反応物(R)-2-(5-methyl-1,2,4-oxadiazol-3-yl)but-3-yn-2-olHCID 86669593—
反応物HCID 178422860HCID 178422860—
生成物HCID 178422861HCID 178422861—

反応手順

10-bromo-9-fluoro-3-iodo-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide was reacted with (2-tert-butoxycarbonyl-5-methyl-pyrazol-3-yl)boronic acid similarly to as described in Example 4 to produce crude 10-bromo-9-fluoro-3-(3-methyl-1H-pyrazol-5-yl)-5,6dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide. 10-bromo-9-fluoro-3-(3-methyl-1H-pyrazol-5-yl)-5,6dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide was reacted with (2R)-2-(5-methyl-1,2,4-oxadiazol-3-yl)but-3-yn-2-ol via General Procedure E to afford 5.8 mg (6.6%) 9-fluoro-10-[(3R)-3-hydroxy-3-(5-methyl-1,2,4-oxadiazol-3-yl)but-1-ynyl]-3-(3-methyl-1H-pyrazol-5-yl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide following reverse phase purification. M+1=478.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09034866B2
出典データセットuspto-grants-2015_05
ORD IDord-218afa56868b4151b112229c7f1bfec6
出典メモuspto-grants-2015_05