反応式
[CH3:1][C@H]1OC(=O)C2C(O)=CC(O)=C(Cl)C=2CC(=O)C=CC=C[C@H]2O[C@H]2C1.C(O)(=O)CCCCCCCCCCCCCCC.[CH:44]1([N:50]=[C:51]=[N:52][CH:53]2[CH2:58][CH2:57][CH2:56]CC2)CCCCC1>O1CCCC1>[CH3:1][N:50]([C:51]1[CH:56]=[CH:57][CH:58]=[CH:53][N:52]=1)[CH3:44]参加物
5
実験手順
Following a procedure similar to that described in Example 12, but using 364 mg of radicicol, 384 mg of palmitic acid, 15 ml of dry tetrahydrofuran, 309 mg of dicyclohexylcarbodiimide and a catalytic amount of dimethylaminopyridine, 62 mg of the title compound were obtained.
出典と根拠
- ORDレコード
- ord-95cb0e4d69ad4219994ad817ae6e22e3
- 出典データセット
- uspto-grants-1997_01
- 特許番号
- US05597846
関連ノート
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