Ammonium Chloride → HCID 11688077, compound
Reaction equation
[N-:1]=[N+:2]=[N-:3].[Na+].[CH2:5]([O:12][C:13]([N:15]1[C@H:22]([CH3:23])[CH2:21][CH2:20][C@H:19]2[C@H:17]([O:18]2)[CH2:16]1)=[O:14])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[Cl-].[NH4+]>CO.O>[CH2:5]([O:12][C:13]([N:15]1[CH2:16][C@@H:17]([OH:18])[C@H:19]([N:1]=[N+:2]=[N-:3])[CH2:20][CH2:21][C@H:22]1[CH3:23])=[O:14])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Sodium azide (1.8 g, 27.7 mmol) was added to a (1R,4R,7S)-4-Methyl-8-oxa-3-aza-bicyclo[5.1.0]octane-3-carboxylic acid benzyl ester (2.4 g, 9.2 mmol, Example 1e) and ammonium chloride (1.48 g, 27.7 mmol) in MeOH (16 ml) and H2O (1.6 ml), then was refluxed overnight. The reaction mixture was concentrated in vacuo by rotary evaporation, then was diluted with water (5 ml) and extracted with EtOAc (10 ml). The organic layer was then extracted with water, brine, dried with MgSO4, filtered, concentrated in vacuo by rotary evaporation, and chromatographed (silica gel, 25% EtOAc/hexanes) to yield the title compound (1.76 g, 63%); Liquid chromatgraphy/Electrospray mass spec: M+H+=305.2.
Workup
- temperaturewas refluxed overnight
- concentrationThe reaction mixture was concentrated in vacuo by rotary evaporation
- additionwas diluted with water (5 ml)
- extractionextracted with EtOAc (10 ml)
- extractionThe organic layer was then extracted with water, brine
- dry with materialdried with MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo by rotary evaporation
- customchromatographed (silica gel, 25% EtOAc/hexanes)
Sources & evidence
- ORD record
- ord-a5a332bfb4d14bbeb535d7313755e407
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07563784B2
Reaction notes
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