Reaction equation
C(N(CC)CC)C.[CH2:8](CN)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)[C:28]2C=CC=[CH:32][C:27]=2N=N1.[C:44]([O:47]CC)(=[O:46])[CH3:45]>C(Cl)Cl>[CH2:8]([O:47][C:44](=[O:46])[CH2:45][CH:27]([CH3:32])[CH3:28])[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1Participants
Procedure
To a solution of 2-(R)-2-[carboxymethyl(4-methoxybenzenesulfonyl)amino]-3-methylbutyric acid benzyl ester (Example 1) (1.05 grams, 2.41 mmol) in methylene chloride (20 mL) were added sequentially triethylamine (0.84 mL, 6.0 mmol),N-benzylmethylamine (0.34 mL, 2.63 mmol) and (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (1.17 grams, 2.69 mmol). The mixture was stirred at room temperature overnight and then diluted with ethyl acetate. The solution was washed with 0.5N hydrochloric acid solution and brine, dried over magnesium sulfate and concentrated under vacuum. The residue was chromatographed on silica gel using 35% ethyl acetate in hexane (plus a small amount of methylene chloride to load the sample on the column) affording 2-(R)-2-[benzylmethylcarbamoylmethyl)(4-methoxybenzenesulfonyl)amino]-3-methylbutyric acid benzyl ester as a clear oil, 1.14 grams (88%).
Workup
- washThe solution was washed with 0.5N hydrochloric acid solution and brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under vacuum
- customThe residue was chromatographed on silica gel using 35% ethyl acetate in hexane (plus a small amount of methylene chloride
Sources & evidence
- ORD record
- ord-1c301499333d4c0b96ddb53ab9809753
- Source dataset
- uspto-grants-1999_01
- Patent number
- US05863949
Linked notes
Loading…