Ethyl 4-methyl-2-(2-oxo-3-phenylimidazolidin-1-yl)thiazole-5-carboxylate → HCID 178504113, compound

HRID 560601Notes

Reaction equation

HRID 560601 reaction equation
[CH3:1]C1N=C(N2CCN(C3C=CC=CC=3)C2=O)SC=1C(OCC)=O.[CH2:24]([C@@H:31]1[CH2:35][N:34]([C:36]2[S:37][C:38]([C:42]([O:44]CC)=[O:43])=[C:39](C)[N:40]=2)[C:33](=[O:47])[NH:32]1)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[CH2:24]([C@@H:31]1[CH2:35][N:34]([C:36]2[SH:37]([CH3:1])[C:38]([C:42]([OH:44])=[O:43])=[CH:39][N:40]=2)[C:33](=[O:47])[NH:32]1)[C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1

Participants

3

Reactant 2

HCID 58031446Ethyl 4-methyl-2-(2-oxo-3-phenylimidazolidin-1-yl)thiazole-5-carboxylateHCID 73213190(R)-ethyl 2-(4-benzyl-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylate

Product 1

HCID 178504113HCID 178504113, compoundYield 83%

Procedure

Following the procedure as described in Example 6, making variations as required to replace ethyl 4-methyl-2-(2-oxo-3-phenylimidazolidin-1-yl)thiazole-5-carboxylate with (R)-ethyl 2-(4-benzyl-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylate, the title compound was obtained in 83% yield: MS (ES+) m/z 318.1 (M+1).

Sources & evidence

ORD record
ord-3f7482af9ed247c185f36447945c43ce
Source dataset
uspto-grants-2011_11
Patent number
US08063084B2

Reaction notes

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