Benzaldehyde → HCID 178519470, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][C:4]1[N:8]=[CH:7][NH:6][CH:5]=1.[C:9]([C:17]1[CH:25]=[CH:24][CH:23]=[CH:22][C:18]=1[C:19]([OH:21])=O)(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[CH:26](=O)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1.[C:34]1([CH:40]([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)[CH2:41][N+:42]#[C-:43])[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1.C[OH:51]>>[C:9]([C:17]1[CH:25]=[CH:24][CH:23]=[CH:22][C:18]=1[C:19]([N:1]([CH:26]([C:43](=[O:51])[NH:42][CH2:41][CH:40]([C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=1)[C:44]1[CH:45]=[CH:46][CH:47]=[CH:48][CH:49]=1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[CH2:2][CH2:3][C:4]1[N:8]=[CH:7][NH:6][CH:5]=1)=[O:21])(=[O:16])[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1Participants
6
Procedure
A solution of histamine (1.11 g, 10.0 mmol), 2-benzoylbenzoic acid (2.26 g, 10.0 mmol), benzaldehyde (1.06 g, 10.0 mmol) and the product of step 1 (2.07 g, 10.0 mmol) in methanol was heated at reflux overnight. The reaction was concentrated and the residue partitioned between ethyl acetate and aqueous sodium bicarbonate solution. The organic layer was dried (sodium sulfate) and concentrated to afford a foamy light brown solid. Flash chromatography over silica (methylene chloride/methanol) afforded 2.99 g (47%) of the product as a beige solid: 1H NMR (CDCl3) δ 7.88–6.84 (m, 25H), 6.65–6.25 (m, 2H), 5.66–5.30 (m, 1H), 4.44–4.20 (m, 1H), 4.17–3.84 (m, 2H), 3.47–3.03 (m, 2H), 2.69–2.18 (m, 2H) ppm. MS (ESI) m/z 634 (M+H+).
Workup
- temperatureat reflux overnight
- concentrationThe reaction was concentrated
- customthe residue partitioned between ethyl acetate and aqueous sodium bicarbonate solution
- dry with materialThe organic layer was dried (sodium sulfate)
- concentrationconcentrated
- customto afford a foamy light brown solid
Sources & evidence
- ORD record
- ord-e2783dcfa6144e5e847c68f6f464533c
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07034031B2
Reaction notes
Loading…