2-(2-Amino-4-thiazolyl)-2-(1-diphenylmethoxycarbonyl-1-methylethoxy)imino acetic acid, hydrochloride salt → (2-Amino-1,3-thiazol-4-YL)({[1-(diphenylmethoxy)-2-methyl-1-oxopropan-2-YL]oxy}imino)acetic acid
Reaction equation
Cl.[NH2:2][C:3]1[S:4][CH:5]=[C:6]([C:8](=[N:12][O:13][C:14]([C:17]([O:19][CH:20]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[O:18])([CH3:16])[CH3:15])[C:9]([OH:11])=[O:10])[N:7]=1>O>[NH2:2][C:3]1[S:4][CH:5]=[C:6]([C:8](=[N:12][O:13][C:14]([C:17]([O:19][CH:20]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=2)=[O:18])([CH3:16])[CH3:15])[C:9]([OH:11])=[O:10])[N:7]=1Participants
3
Procedure
A suspension of the hydrochloride salt product from part (e) in water (20 ml./g.) is adjusted to pH 2.6 and stirred for 30 minutes at 0°. The resulting suspension is filtered, washed thoroughly with water, and dried to yield 2-(2-amino-4-thiazolyl)-2-(1-diphenylmethoxycarbonyl-1-methylethoxy)iminoacetic acid.
Workup
- filtrationThe resulting suspension is filtered
- washwashed thoroughly with water
- customdried
Sources & evidence
- ORD record
- ord-c10006c316754e7cbd3b5f6d41acb96a
- Source dataset
- uspto-grants-1980_12
- Patent number
- US04237128
Reaction notes
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