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HRID 2264586作成日:2026年10月27日

Sodium cyanoborohydride → 5-(6-Chloro-pyrimidin-4-yloxy)-2,3-dihydro-indole

https://huagongshe.com/reaction/2264586

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium cyanoborohydrideHCID 5003444—
反応物5-((6-Chloropyrimidin-4-yl)oxy)-1H-indoleHCID 57455156—
溶媒Acetic AcidHCID 176—
生成物5-(6-Chloro-pyrimidin-4-yloxy)-2,3-dihydro-indoleHCID 85891628—

反応手順

A solution of 246 mg (1.0 mMol) of 5-(6-chloro-pyrimidin-4-yloxy)-1H-indole (WO 03/099771; Stage 163.1) in 5.5 ml acetic acid is cooled to 10-15° C. Then 314 mg (5 mMol) NaBH3CN are added portionwise. After 1 h stirring, 9 g of ice are added and the mixture is concentrated partially in vacuo. The residue is dissolved in 25 ml 1 N NaOH and extracted three times with EtOAc. The organic layers are washed twice with water and brine, dried (Na2SO4) and concentrated at rt in vacuo: MS: [M+1]+=248; TLC(EtOAc/hexane 1:1): Rf=0.31.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07855215B2
出典データセットuspto-grants-2010_12
ORD IDord-87a0ceb01dc54bf09ee1d6020920e641
出典メモuspto-grants-2010_12