Benzoic acid, 3-ethyl- → 2-(5-Carbamimidoyl-2-((3-ethylbenzamido)methyl)phenylamino)acetic acid
Reaction equation
Cl.[NH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:14]=C(C)O[N:11]=2)=[CH:6][C:5]=1[NH:16][CH2:17][C:18]([O:20]CC1C=CC=CC=1)=[O:19].[CH2:28]([C:30]1[CH:31]=[C:32]([CH:36]=[CH:37][CH:38]=1)[C:33](O)=[O:34])[CH3:29]>>[C:10]([C:7]1[CH:8]=[CH:9][C:4]([CH2:3][NH:2][C:33](=[O:34])[C:32]2[CH:36]=[CH:37][CH:38]=[C:30]([CH2:28][CH3:29])[CH:31]=2)=[C:5]([NH:16][CH2:17][C:18]([OH:20])=[O:19])[CH:6]=1)(=[NH:11])[NH2:14]Participants
3
Procedure
Compound 58d was reacted with 3-ethylbenzoic acid and subsequently hydrogenated according to the procedure described in Example 58, to give Example 59. ESI-MS m/e 355.5 (M+1).
Workup
- customto give Example 59
Sources & evidence
- ORD record
- ord-166b72b2c6c746488ba25c9ee473301a
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07247654B2
Reaction notes
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