反应 #543567

ord-ccb0ea35762f4351893693de985e55d3

反应方程式

O=C(Cl)N1CCNC1=O
2-oxo-imidazolidine-1-carbonyl chloride
COc1ccc(C2=NN(C3CCN(C(=O)N4CCOCC4)CC3)C(=O)[C@H]3CC=CC[C@@H]23)cc1Cl
compound 1
COc1ccc(C2=NN(C3CCN(C(=O)N4CCOCC4)CC3)C(=O)[C@H]3CC=CC[C@@H]23)cc1Cl
(cis)-4-(3-Chloro-4-methoxy-phenyl)-2-[1-(1-morpholin-4-yl-methanoyl)-piperidin-4-yl]-4a,5,8,8a-tetrahydro-2H-phthalazin-1-one
COc1ccc(C2=NN(C3CCN(C(=O)N4CCNC4=O)CC3)C(=O)[C@H]3CC=CC[C@@H]23)cc1Cl
cis-4-(3-Chloro-4-methoxy-phenyl)-2-{1-[1-(2-oxo-imidazolidin-1-yl)-methanoyl]-piperidin-4-yl}-4a,5,8,8a-tetrahydro-2H-phthalazin-1-one

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Prepared from intermediate product A1 and 2-oxo-imidazolidine-1-carbonyl chloride as described for compound 1. M. p. 216–218° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07186710B2uspto-grants-2007_03