Proline benzyl ester hydrochloride → HCID 68577764, compound
Reaction equation
[O:1]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[NH:14][S:15]([C:18]1[CH:30]=[CH:29][C:21]([C:22]([NH:24][CH2:25][C:26]([OH:28])=O)=[O:23])=[CH:20][CH:19]=1)(=[O:17])=[O:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[CH2:32]([O:39][C:40](=[O:46])[C@@H:41]1[CH2:45][CH2:44][CH2:43][NH:42]1)[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1>>[CH2:32]([O:39][C:40]([C@@H:41]1[CH2:45][CH2:44][CH2:43][N:42]1[C:26](=[O:28])[CH2:25][NH:24][C:22](=[O:23])[C:21]1[CH:20]=[CH:19][C:18]([S:15](=[O:17])(=[O:16])[NH:14][C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[O:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)=[CH:30][CH:29]=1)=[O:46])[C:33]1[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=1Participants
3
Procedure
The title compound was prepared from [4-(2-phenoxy-phenylsulfamoyl)-benzoylamino]-acetic acid and L-proline benzyl ester hydrochloride according to the method described in Example 1.1/d. MS (EI) 614.3 (MH+).
Sources & evidence
- ORD record
- ord-7a9d6178c45840289d2c069cb9417d28
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08481527B2
Reaction notes
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