反応式
[OH:1][C@H:2]1[C@H:16](/[CH:17]=[CH:18]/[CH2:19][C:20]([OH:26])([CH3:25])[CH2:21][CH2:22][CH2:23][CH3:24])[C@@H:5]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]([O:14]C)=[O:13])[C:4](=[O:27])[CH2:3]1.[CH2:28](O)C(N)(CO)CO>>[CH3:28][CH:11]([CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][C@@H:5]1[C@@H:16](/[CH:17]=[CH:18]/[CH2:19][C:20]([OH:26])([CH3:25])[CH2:21][CH2:22][CH2:23][CH3:24])[C@H:2]([OH:1])[CH2:3][C:4]1=[O:27])[C:12]([OH:14])=[O:13]参加物
3
実験手順
To a stirred suspension of 3.1 g of (±) methyl 11α,16-dihydroxy-16-methyl-9-oxoprost-13E-en-1-oate in 20 ml Tris buffer (pH 8.0) is added 50 ml porcine liver esterase (Sigma, St. Louis, Mo.). After 3 hours of stirring at room temperature, the reaction is extracted with 4 portions of ethyl acetate, the extracts combined, dried (Na2SO4), evaporated and chromatographed on silica gel to give 2.8 g of (±) methyl 11α,16-dihydroxy-16-methyl-9-oxoprost-13E-en-1-oic acid.
後処理
- additionis added 50 ml porcine liver esterase (Sigma, St. Louis, Mo.)
- extractionthe reaction is extracted with 4 portions of ethyl acetate
- dry with materialdried (Na2SO4)
- customevaporated
- customchromatographed on silica gel
出典と根拠
- ORDレコード
- ord-113c83e1b46849c6a1585ff4034b7468
- 出典データセット
- uspto-grants-1992_10
- 特許番号
- US05157052
関連ノート
読み込み中…