Ammonium Chloride → HCID 22260279, compound
Reaction equation
[CH3:1][C:2]1([CH3:23])[C:7]2[CH:8]=[C:9]([C:12]3[NH:16][C:15]([C:17]#[N:18])=[C:14]([N+:19]([O-])=O)[CH:13]=3)[CH:10]=[CH:11][C:6]=2[NH:5][C:4](=[O:22])[O:3]1.[NH4+].[Cl-]>CCO.O.C(OCC)(=O)C.[Zn]>[NH2:19][C:14]1[CH:13]=[C:12]([C:9]2[CH:10]=[CH:11][C:6]3[NH:5][C:4](=[O:22])[O:3][C:2]([CH3:1])([CH3:23])[C:7]=3[CH:8]=2)[NH:16][C:15]=1[C:17]#[N:18]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Conditions
- Temperature
- 60 °C
Procedure
To 5-(4,4-dimethyl-2-oxo-1,4-dihydro-2H-3,1 -benzoxazin-6-yl)-3-nitro-1H-pyrrole-2-carbonitrile (0.14 g, 0.45 mmol) in EtOH/H2O (5:1, 20 mL:4 mL) was added Zn powder (0.35 g, 5.3 mmol) and NH4Cl (0.70 g, 13 mmol) and the mixture was heated to 60° C. for 25 min. After cooling to room temperature and stirring 24 h, the reaction mixture was diluted with ethyl acetate (100 mL) and filtered through a pad of celite. The filtrate was washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by flash column chromatography (60% ethyl acetate/hexane) on silica gel gave the product as an orange foam (30 mg, 24%). 1H NMR (500 MHz, d6-DMSO) δ 1.63 (s, 6H), 5.01 (s, 2H), 5.95 (d, 1H, J=2.9 Hz), 6.87 (d, 1H, J=8.3 Hz), 7.48 (dd, 1H, J=2.0, 8.3 Hz), 7.54 (d, 1H, J=2.0 Hz), 10.30 (s, 1H), 11.17 (d, 1H, J=2.5 Hz). MS (ESI) [M−H]− m/z 281.
Workup
- temperatureAfter cooling to room temperature
- filtrationfiltered through a pad of celite
- washThe filtrate was washed with water (50 mL) and brine (50 mL)
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customPurification by flash column chromatography (60% ethyl acetate/hexane) on silica gel
Sources & evidence
- ORD record
- ord-28c1ece98d2e4274912fb82c1d6d4593
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06982261B2
Reaction notes
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