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HRID 595448作成日:2026年10月24日

Diisobutylaluminum hydride → (6-Chloro-4-(isopropylamino)pyridin-3-yl)methanol

https://huagongshe.com/ja/reaction/595448

反応式

関与物質

役割名称HCID仕込み量
反応物Diisobutylaluminum hydrideHCID 14487—
反応物Ethyl 6-chloro-4-(cyclobutylamino)nicotinateHCID 89689654—
溶媒DichloromethaneHCID 6344—
生成物(6-Chloro-4-(isopropylamino)pyridin-3-yl)methanolHCID 89689798—

反応条件

温度-78 °C

反応手順

To a stirred solution of ethyl 6-chloro-4-(isopropylamino)nicotinate (2) (1 g, 4.12 mmol) in dry DCM (30 mL), DIBAL-H (8.24 mmol, 2 equiv.) (1.0 M in DCM) was added dropwise at −78° C. The reaction mixture was stirred at −78° C. for 2 h, gradually, the reaction was allowed to warm up to −10° C. over 1 h. The reaction mixture was quenched with saturated solution of sodium potassium tarterate and allowed to stir at room temperature. The reaction mixture was filtered through a small pad of celite. The filtrate was washed with brine solution, dried over Na2SO4, filtered and concentrated to give crude alcohol. The crude material obtained was purified by flash column chromatography through silica gel and MeOH: CHCl3 as eluent to afford (6-chloro-4-(isopropylamino)pyridin-3-yl)methanol. LC/MS: ZORBAX SB C18, 4.6×50 mm, 5 μm; Solvent A=10% MeOH: 90% H2O: 0.1% TFA; Solvent B=90% MeOH: 10% H2O: 0.1% TFA; gradient 0-100% B over 2 min (3 min run time); retention time: 0.806 min; LCMS (ES-API), m/z 201.0 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242975B2
出典データセットuspto-grants-2016_01
ORD IDord-60859828119e4b81b1353469623e850a
出典メモuspto-grants-2016_01