HCID 88498842, compound → HCID 88498867, compound
Reaction equation
[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:36]/[O:37][CH3:38])/[C:8]([NH:10][C@@H:11]2[C:18](=[O:19])[N:17]3[C@@H:12]2[S:13][CH2:14][C:15]([CH2:23][S:24][C:25]2[N:30]4[N:31]=[CH:32][N:33]=[C:29]4[N:28]=[C:27](OC)[CH:26]=2)=[C:16]3[C:20]([OH:22])=[O:21])=[O:9])[N:6]=1.NC1SC=C(/C(=N/OC)/C(N[C@@H]2C(=O)N3[C@@H]2SCC(CSC2N4N=C(N)N=C4N=C(C)C=2)=C3[C:58]([OH:60])=[O:59])=O)N=1>>[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:36]/[O:37][CH3:38])/[C:8]([NH:10][C@@H:11]2[C:18](=[O:19])[N:17]3[C@@H:12]2[S:13][CH2:14][C:15]([CH2:23][S:24][C:25]2[N:30]4[N:31]=[C:32]([C:58]([OH:60])=[O:59])[N:33]=[C:29]4[N:28]=[CH:27][CH:26]=2)=[C:16]3[C:20]([OH:22])=[O:21])=[O:9])[N:6]=1Participants
3
Procedure
(6R,7R)-7-[2-(2-amino-4-thiazolyl)-2-(Z-methoxyimino)acetamido]-3-[(5-methoxy-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Compound 17: (6R,7R)-7-[2-(2-amino-4-thiazolyl)-2-(Z-methoxyimino)acetamido]-3-[(2-amino-5-methyl-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Sources & evidence
- ORD record
- ord-c70727941d894ed294d2e6a84d0f050a
- Source dataset
- uspto-grants-1991_11
- Patent number
- US05064953
Reaction notes
Loading…