Triethylamine → HCID 18660145、化合物
反応式
[OH:1][CH2:2][C@@H:3]1[CH2:7][CH2:6][CH2:5][N:4]1[C:8](=[O:13])[C:9]([F:12])([F:11])[F:10].C(N(CC)CC)C.[CH3:21][S:22](Cl)(=[O:24])=[O:23]>C(Cl)Cl>[CH3:21][S:22]([O:1][CH2:2][C@@H:3]1[CH2:7][CH2:6][CH2:5][N:4]1[C:8](=[O:13])[C:9]([F:10])([F:11])[F:12])(=[O:24])=[O:23]参加物
5
実験手順
To a solution of the product of step A (1.002 g, 5.08 mmol) and triethylamine (0.78 ml, 5.60 mmol) in CH2Cl2 (50 ml) at -25° C. was added methane sulfonyl chloride (0.40 ml, 5.17 mmol) over a period of 5 min and stirring was continued for 1 hr. The solvent was evaporated in vacuo and the residue purified by chromatography (SiO2, 33% EtOAc in hexanes, elution). The title compound was obtained as a colorless oil.
後処理
- customThe solvent was evaporated in vacuo
- customthe residue purified by chromatography (SiO2, 33% EtOAc in hexanes, elution)
出典と根拠
- ORDレコード
- ord-de57cc5c14204dbe86b4d2a7aa4e0de7
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05756528
反応ノート
読み込み中…