HCID 68838489, compound → HCID 57777388, compound

HRID 660628Notes

Reaction equation

HRID 660628 reaction equation
C([O:8][C:9]1[CH:10]=[C:11](/[CH:23]=[CH:24]/[C:25]([OH:27])=O)[CH:12]=[CH:13][C:14]=1[N:15]1[CH2:19][C:18](=[O:20])[NH:17][S:16]1(=[O:22])=[O:21])C1C=CC=CC=1.C([O:35][C:36]1[C:37]([S:48]([CH3:50])=[O:49])=[C:38]([CH:45]=[CH:46][CH:47]=1)[O:39][CH2:40][CH2:41][CH2:42][CH2:43][NH2:44])C1C=CC=CC=1>>[OH:35][C:36]1[C:37]([S:48]([CH3:50])=[O:49])=[C:38]([CH:45]=[CH:46][CH:47]=1)[O:39][CH2:40][CH2:41][CH2:42][CH2:43][NH:44][C:25](=[O:27])[CH2:24][CH2:23][C:11]1[CH:12]=[CH:13][C:14]([N:15]2[CH2:19][C:18](=[O:20])[NH:17][S:16]2(=[O:21])=[O:22])=[C:9]([OH:8])[CH:10]=1

Participants

3

Procedure

The title compound is prepared using (E)-3-[3-benzyloxy-4-(1,1,4-trioxo-1,2,5-thiadiazolidin-2-yl)-phenyl]-acrylic acid and 4-(3-benzyloxy-2-methanesulfinylphenoxy)-butylamine analogous to Example 100 steps C and D: (M−1)−=524. HPLC retention time: 0.89 min. (Method A).

Sources & evidence

ORD record
ord-aca2b5567a53429782ca3ffd95b0778c
Source dataset
uspto-grants-2011_12
Patent number
US08084448B2

Reaction notes

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