(7R,7aS)-4-(7-Hydroxy-1,3-dioxotetrahydropyrrolo[1,2-c]imidazol-2-yl)-5,6,7,8-tetrahydronaphthalene-1-carbonitrile → HCID 59754298, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]([CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:7](=[O:19])[CH:6]=[CH:5]2.N(C1C2CCCCC=2C(C#N)=CC=1)=C=O.[OH:35][C@H:36]1[C@@H:43]2[N:39]([C:40](=[O:57])N(C3C4CCCCC=4C(C#N)=CC=3)[C:42]2=[O:44])[CH2:38][CH2:37]1>>[OH:35][C@H:36]1[C@@H:43]2[N:39]([C:40](=[O:57])[N:1]([C:2]3[CH:3]=[C:4]4[C:9](=[CH:10][CH:11]=3)[N:8]([CH2:12][C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=3)[C:7](=[O:19])[CH:6]=[CH:5]4)[C:42]2=[O:44])[CH2:38][CH2:37]1Participants
4
Procedure
The title compound was prepared from compound 46D by procedures analogous to those described in Experiment 2E and 2F. LC/MS m/z 390 [M+H]+.
Sources & evidence
- ORD record
- ord-483c4677941e48298aacb27fb958df9e
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07405234B2
Reaction notes
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