4-Amino-1-butanol → HCID 58990025, compound
Reaction equation
[CH2:1]([O:8][NH:9][C:10]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[NH:18][CH2:19][C:20]1[CH:21]=[CH:22][C:23]([F:29])=[C:24]([CH:28]=1)[C:25]([OH:27])=O)=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:30][CH2:31][CH2:32][CH2:33][CH2:34][OH:35]>>[CH2:1]([O:8][NH:9][C:10]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[NH:18][CH2:19][C:20]1[CH:21]=[CH:22][C:23]([F:29])=[C:24]([CH:28]=1)[C:25]([NH:30][CH2:31][CH2:32][CH2:33][CH2:34][OH:35])=[O:27])=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
Prepared by a similar procedure as described for the preparation of Example 499, starting from 5-[(2-benzyloxycarbamoyl-phenylamino)methyl]-2-fluoro-benzoic acid (Example 498) and 4-amino-butan-1-ol.
Workup
- customPrepared by a similar procedure
- customas described for the preparation of Example 499
Sources & evidence
- ORD record
- ord-1ca6eb7b2c264221a78bb06ec5b4583b
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08034811B2
Reaction notes
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