反応式
S(Cl)([Cl:3])=O.[NH2:5][C@@H:6]([C:14]([OH:16])=[O:15])[CH2:7][CH:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.Cl.[CH3:18]O>>[NH2:5][C@@H:6]([C:14]([O:16][CH3:18])=[O:15])[CH2:7][CH:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.[ClH:3]参加物
4
実験手順
To cold (−20° C.) and dry methanol (195 ml) was added dropwise thionylchloride (28 ml). H—D—Cha—OH.HCl (40 g) was added and the reaction mixture was heated under reflux for 5 hours The mixture was concentrated in vacuo and coevaporated with methanol (3 times). The residue was crystallized from methanol/diethyl ether yielding H—D—Cha—OMe.HCl as a white crystalline powder (40.9 g). TLC: Rf=0.66, silica gel, n-butanol/acetic acid/water 10/1/3 v/v/v.
後処理
- temperaturethe reaction mixture was heated
- temperatureunder reflux for 5 hours The mixture
- concentrationwas concentrated in vacuo
- customThe residue was crystallized from methanol/diethyl ether
出典と根拠
- ORDレコード
- ord-0cd394abdff64075b31e61d342bdef49
- 出典データセット
- uspto-grants-2001_04
- 特許番号
- US06218365B1
関連ノート
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