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HRID 1815963作成日:2026年10月27日

1,1-Dibromoethane → 1-Bromo-3-[7-bromo-1-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-propyl]-1H-indazol-6-yloxy]-propan-2-ol

https://huagongshe.com/reaction/1815963

反応式

関与物質

役割名称HCID仕込み量
反応物1,1-DibromoethaneHCID 11201—
反応物MagnesiumHCID 5462224—
反応物7-Bromo-1-[(S)-2-(tert-butyldimethyl-silanyloxy)-propyl]-6-oxiranylmethoxy-1H-indazoleHCID 86759649—
溶媒TetrahydrofuranHCID 8028—
生成物1-Bromo-3-[7-bromo-1-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-propyl]-1H-indazol-6-yloxy]-propan-2-olHCID 6956428095.3%

反応条件

温度50 °C

反応手順

To a suspension of magnesium powder (0.73 g, 30.2 mmol) in anhydrous THF (50 mL) under nitrogen was added dibromoethane (2.13 g, 0.98 mL, 11.3 mmol) in portions over about 30 min. During this period the mixture was heated at about 50° C. until gas evolution was observed. The mixture was stirred for an additional 1 h, placed in an ice bath, and a solution of the product from Step D (3.33 g, 7.55 mmol) in THF (10 mL) was added. After stirring for 1 h at ambient temperature, the mixture was quenched with a saturated aqueous solution of ammonium chloride (100 mL) and extracted with EtOAc (3×100 mL). Evaporation of the extracts gave a crude oil (3.76 g, 95%): LC/MS (+APCI) m/z 441, 443 (M+H−HBr).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06881749B2
出典データセットuspto-grants-2005_04
ORD IDord-3ad693654e834867a58c503ce29cc182
出典メモuspto-grants-2005_04