HCID 12942918, compound → HCID 12942924, compound
Reaction equation
COC(C1C([C:11]2[N:12]=[C:13](C3C=CC=CC=3)[S:14][CH:15]=2)C(C(OC)=O)=C(C)NC=1C)=O.[CH:28]([O:31][C:32]([C:34]1[CH:39](C2N=C(C3C=CC=CC=3)SC=2)[C:38]([C:51]([O:53][CH:54]([CH3:56])C)=[O:52])=[C:37]([CH3:57])[NH:36][C:35]=1[CH3:58])=[O:33])([CH3:30])[CH3:29]>>[CH:28]([O:31][C:32]([C:34]1[CH:39]([C:13]2[S:14][CH:15]=[CH:11][N:12]=2)[C:38]([C:51]([O:53][CH2:54][CH3:56])=[O:52])=[C:37]([CH3:57])[NH:36][C:35]=1[CH3:58])=[O:33])([CH3:29])[CH3:30]Participants
3
Procedure
The following compounds were obtained in an analogous manner: (b) 2,6-dimethyl-4-thiazol-2-yl-1,4-dihydropyridine-3,5-dicarboxylic acid 3-ethyl 5-methyl ester and (c) 2,6-dimethyl-4-thiazol-2-yl-1,4-dihydropyridine-3,5-dicarboxylic acid 3-ethyl 5-propyl ester.
Workup
- customThe following compounds were obtained in an analogous manner
Sources & evidence
- ORD record
- ord-caef0e5a40ee4f75a3750fef9012b8ef
- Source dataset
- uspto-grants-1983_04
- Patent number
- US04380547
Reaction notes
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