Ammonium Chloride → HCID 22260279, compound

HRID 444751Notes

Reaction equation

HRID 444751 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

6

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 minutes. After cooling to room temperature and stirring 24 h, the reaction mixture was diluted with ethyl acetate (100 mL) and filtered through a Celite® pad. 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

  1. temperatureAfter cooling to room temperature
  2. filtrationfiltered through a Celite® pad
  3. washThe filtrate was washed with water (50 mL) and brine (50 mL)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customPurification by flash column chromatography (60% ethyl acetate/hexane) on silica gel

Sources & evidence

ORD record
ord-3d802176770b4ba4a3a4a139a9725a19
Source dataset
uspto-grants-2013_07
Patent number
US08476262B2

Reaction notes

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