3-Hydroxybenzoic Acid → HCID 11267863, compound
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].[OH:28][C:29]1[CH:30]=[C:31]([CH:35]=[CH:36][CH:37]=1)[C:32](O)=[O:33]>>[C:10]([C:7]1[CH:8]=[CH:9][C:4]([CH2:3][NH:2][C:32](=[O:33])[C:31]2[CH:35]=[CH:36][CH:37]=[C:29]([OH:28])[CH:30]=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-hydroxybenzoic acid and subsequently hydrogenated according to the procedure described in Example 58, to give example 67. ESI-MS m/e 343.5 (M+1).
Workup
- customto give example 67
Sources & evidence
- ORD record
- ord-01accb74a40842729d2daa12d9baa79b
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07247654B2
Reaction notes
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