Glycine ethyl ester, hydrochloride → HCID 68489603, compound
Reaction equation
[Cl:1][C:2]1[CH:28]=[C:27]([Cl:29])[CH:26]=[CH:25][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[NH:12][S:13]([C:16]1[CH:24]=[CH:23][C:19]([C:20](O)=[O:21])=[CH:18][CH:17]=1)(=[O:15])=[O:14])=[O:5].Cl.[CH2:31]([O:33][C:34](=[O:37])[CH2:35][NH2:36])[CH3:32]>>[CH2:31]([O:33][C:34](=[O:37])[CH2:35][NH:36][C:20](=[O:21])[C:19]1[CH:18]=[CH:17][C:16]([S:13](=[O:14])(=[O:15])[NH:12][C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[C:4](=[O:5])[C:3]2[CH:25]=[CH:26][C:27]([Cl:29])=[CH:28][C:2]=2[Cl:1])=[CH:24][CH:23]=1)[CH3:32]Participants
3
Procedure
The title compound was prepared from 4-[2-(2,4-dichloro-benzoyl)-phenylsulfamoyl]-benzoic acid and glycine ethyl ester hydrochloride according to the method described in Example 1.1/d. MS (EI) 536.1 (MH+).
Sources & evidence
- ORD record
- ord-c83a4f0d57c74fe181a9d38a51e3f312
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08481527B2
Reaction notes
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