Acetic Acid → HCID 178519502, compound
Reaction equation
[CH:1]1([C@@:7](O)([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:8]([NH2:10])=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[OH2:18].[NH2:19][NH2:20].[C:21](O)(=O)C>COC(OC)N(C)C>[CH:1]1([C@@:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)([C:8]2[N:10]=[CH:21][NH:20][N:19]=2)[OH:18])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
Conditions
- Temperature
- 90 °C
Procedure
(2R)-2-cyclohexyl-2-hydroxy-2-phenylacetamide (Preparation 1, 4.497 g, 19.27 mmol) was dissolved in N,N-dimethylformamide dimethylacetal (60 ml). After stirring at 90° C. for 2 hours the solvent was removed in vacuo and residue azeotroped with toluene (100 ml) to give a yellow oil. Hydrazine hydrate (1.11 ml, 22.9 mmol) was added followed by glacial acetic acid (90 ml). After stirring at 90° C. for 2 hours the solvent was removed in vacuo and the residue partitioned between ethyl acetate (250 ml) and saturated aqueous sodium bicarbonate solution (250 mL). The organic layer was separated, dried over magnesium sulphate, filtered and the solvent removed in vacuo. The residue was purified by column chromatography on silica gel eluting with ethyl acetate to furnish the title compound as a white solid, in 100% yield, 4.9 g.
Workup
- customwas removed in vacuo and residue
- customazeotroped with toluene (100 ml)
- customto give a yellow oil
- stirringAfter stirring at 90° C. for 2 hours the solvent
- customwas removed in vacuo
- customthe residue partitioned between ethyl acetate (250 ml) and saturated aqueous sodium bicarbonate solution (250 mL)
- customThe organic layer was separated
- dry with materialdried over magnesium sulphate
- filtrationfiltered
- customthe solvent removed in vacuo
- customThe residue was purified by column chromatography on silica gel eluting with ethyl acetate
Sources & evidence
- ORD record
- ord-91ab652680a14f27a72a9fc2e37f51a4
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263623B2
Reaction notes
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