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HRID2256488

反应详情

EQUATION

反应方程式

HRID 2256488 的结构方程式

REACTANTS

反应物

2
结构：CC(C)c1cc(Oc2c(Cl)cc(NC(=O)C(=O)OCc3ccccc3)cc2Cl)ccc1OC(=O)CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C
HCID22866671

未命名化合物

结构：[H][H]
HCID178418361

未命名化合物

PRODUCTS

生成物

1
结构：CC(C)c1cc(Oc2c(Cl)cc(NC(=O)C(=O)O)cc2Cl)ccc1OC(=O)CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C
HCID22866669

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

2
结构：[C].[Pd]
催化剂HCID178418390

未命名化合物

结构：CCO
溶剂HCID702

Ethanol

C2H6O

PROCEDURE

实验过程

4- {4-[(2-benzyloxy-1,2-dioxoethyl)amino]-2,6-dichlorophenoxy}-2-isopropylphenyl 3,7,12(3α,5β,7α,12α)-trihydroxycholan-24-oate (260 mg) and 26 mg of 10% palladium carbon in 50 ml ethanol are treated with hydrogen on a Parr shaker. Catalyst is removed by filtering through celite and the fitrate is stripped to give 4-{2,6-dichloro4-[(2-hydroxy-1,2-dioxoethyl) amino]phenoxy}-2-isopropylphenyl 3,7,12(3α,5β,7α,12α)-trihydroxycholan-24oate, as an amorphane monohydrate, m.p. 180°-92° (dec.).

WORKUP

后处理

  1. customCatalyst is removed
  2. filtrationby filtering through celite