Acetic Acid → HCID 178437441, compound
Reaction equation
C([O:3][C:4]([C:6]1[N:11]=[C:10]2[N:12]([CH2:17][C:18]3[CH:23]=[CH:22][C:21]([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=4[C:30]4[NH:34][N:33]=[N:32][N:31]=4)=[CH:20][CH:19]=3)[C:13]([CH2:15][CH3:16])=[N:14][C:9]2=[C:8]([CH3:35])[CH:7]=1)=O)C.[NH:36]1[CH2:41][CH2:40][O:39][CH2:38][CH2:37]1.[H-].[Na+].CC(O)=O>C1COCC1>[CH2:15]([C:13]1[N:12]([CH2:17][C:18]2[CH:19]=[CH:20][C:21]([C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=3[C:30]3[NH:34][N:33]=[N:32][N:31]=3)=[CH:22][CH:23]=2)[C:10]2=[N:11][C:6]([C:4]([N:36]3[CH2:41][CH2:40][O:39][CH2:38][CH2:37]3)=[O:3])=[CH:7][C:8]([CH3:35])=[C:9]2[N:14]=1)[CH3:16]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To 5-(ethoxycarbonyl)-2-ethyl-7-methyl-3- (2'-(tetrazol-5-yl)biphen-4-yl)methyl-3H-imidazo[4,5-b]pyridine (30 mg) in THF (1 mL) at RT was added 0.25 mL of morpholine and NaH (20 mg of an 80% dispersion). After stirring for 16 hours, 1% aqueous HOAc (2 mL) was added. Extractive workup (EtOAc), and purification (SiO2, 75/25/1 CH2Cl2 /MeOH/NH4OH) gave 10 mg of a solid. 1H NMR (300 MHz, CD3OD) δ 7.62-7.52 (m, 2 H), 7.50-7.42 (m, 2H), 7.40 (s, 1H), 7.06 (s, 4H), 5.52 (s, 2H), 3.82-3.72 (m, 4H), 3.58-3.46 (m, 4H), 2.94 (q, 2H, J=7.5 Hz), 2.69 (s, 3H),1.30 (t, 3H, J=7.5 Hz)
Workup
- customExtractive workup (EtOAc), and purification (SiO2, 75/25/1 CH2Cl2 /MeOH/NH4OH)
Sources & evidence
- ORD record
- ord-76e42d51440144309648bcd9fc1a404c
- Source dataset
- uspto-grants-1994_07
- Patent number
- US05332744
Reaction notes
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