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HRID1822441

反应详情

EQUATION

反应方程式

HRID 1822441 的结构方程式

REACTANTS

反应物

4
结构：N[C@@H](CO)c1ccccc1
HCID2724025

(R)-beta-Aminophenethyl alcohol

C8H11NO

结构：C=CC1CC1(NC(=O)C1CC(Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)CN1)C(=O)OCC
HCID20765316

未命名化合物

结构：C=CC1CC1(NC(=O)C1CC(Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)CN1C(=O)NC(C(=O)NC1c2ccccc2CC1O)C(C)(C)C)C(=O)OCC
HCID68491628

未命名化合物

结构：C=CC1CC1(C(=O)O)C1CC(Oc2cc(-c3ccccc3)cc3cc(OC)ccc23)CN1C(C(=O)NC1c2ccccc2CC1O)C(C)(C)C
HCID68493461

未命名化合物

PRODUCTS

生成物

1
结构：C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H](Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)CN1C(=O)N[C@@H](CO)c1ccccc1)C(=O)O
HCID68492989

未命名化合物

PROCEDURE

实验过程

Compound 12 was treated as described for the preparation of 13 but with the use of (R)-2-phenylglycinol instead of 2-amino-N-(2-hydroxyindan-1-yl)-3,3-dimethyl butyramide instead of 2-amino-N-(2-hydroxy-indan-1-yl)-3,3-dimethyl-butyramide followed by ester hydrolysis as described for the preparation of compound 14 which gave the title compound. Purity by HPLC>95%. M+H+637.1.