Chlorotrimethylsilane → 3-Trimethylsilyl-L-alanine methyl ester hydrochloride
反応式
C(OC([NH:8][C@H:9]([C:15]([OH:17])=[O:16])[CH2:10][Si:11]([CH3:14])([CH3:13])[CH3:12])=O)(C)(C)C.[CH3:18][Si]([Cl:22])(C)C>CO>[ClH:22].[CH3:18][O:17][C:15](=[O:16])[C@H:9]([CH2:10][Si:11]([CH3:12])([CH3:13])[CH3:14])[NH2:8]参加物
4
反応条件
- 温度
- 0 °C
実験手順
The compound of Example 6A (300 mg) is dissolved in methanol (3 ml) and cooled to 0° C. Trimethylsilyl chloride (590 mg, 4.7 eq.) is added dropwise in the course of 30 min. and the mixture is warmed to RT overnight. The volatile components are removed on a Rotavapor and subsequently under high vacuum. The target compound (224 mg, 92% of th.) is obtained.
後処理
- temperaturethe mixture is warmed to RT overnight
- customThe volatile components are removed on a Rotavapor and subsequently under high vacuum
- customThe target compound (224 mg, 92% of th.) is obtained
出典と根拠
- ORDレコード
- ord-973258b32ab84a219a5fabe31279058c
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07727956B2
反応ノート
読み込み中…