Octylamine → 2-hydroxy-5-({{4-[(octylamino)carbonyl]benzyl}[(2E)-3-phenylprop-2-enoyl]amino}methyl)benzoic acid
Reaction equation
[CH2:1]([NH2:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].Cl[CH2:11][C:12]1[CH:20]=[CH:19][C:15]([C:16](Cl)=[O:17])=[CH:14][CH:13]=1.[C:21]1(/[CH:27]=[CH:28]/[C:29](Cl)=[O:30])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.C(O)(=O)C.[NH2:36][CH2:37][C:38]1[CH:50]=[CH:49][C:41]2[O:42]C(C)(C)[O:44][C:45](=[O:46])[C:40]=2[CH:39]=1>>[OH:42][C:41]1[CH:49]=[CH:50][C:38]([CH2:37][N:36]([CH2:11][C:12]2[CH:20]=[CH:19][C:15]([C:16]([NH:9][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])=[O:17])=[CH:14][CH:13]=2)[C:29](=[O:30])/[CH:28]=[CH:27]/[C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[CH:39][C:40]=1[C:45]([OH:46])=[O:44]Participants
5
Procedure
The title compound was prepared following the procedure A using octylamine, 4-(chloromethyl)benzoyl chloride, (2E)-3-phenylacryloyl chloride and 6-(aminomethyl)-2,2-dimethyl-4H-1,3-benzodioxin-4-one acetate. M+(ESI): 543.5
Sources & evidence
- ORD record
- ord-1066375f13d24261bf178a3fc836c0cd
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365225B2
Reaction notes
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