Acetic Acid → (2S,6RS)-4-(4-amino-quinazolin-7-ylmethyl)-2,6-dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl ester
Reaction equation
C(O)(=O)C.[N:5]1[CH:10]=[N:9][CH:8]=[N:7][CH:6]=1.[CH2:11]([O:18][C:19]([N:21]1[CH:26]([CH3:27])[CH2:25][N:24]([CH2:28][C:29]2[CH:34]=C[C:32](C#N)=[C:31](N)[CH:30]=2)[C:23](=[O:38])[C@@H:22]1[CH3:39])=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(OCC)(=O)C>C(O)C>[CH2:11]([O:18][C:19]([N:21]1[CH:26]([CH3:27])[CH2:25][N:24]([CH2:28][C:29]2[CH:34]=[C:6]3[C:32]([C:10]([NH2:5])=[N:9][CH:8]=[N:7]3)=[CH:31][CH:30]=2)[C:23](=[O:38])[C@@H:22]1[CH3:39])=[O:20])[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Glacial acetic acid (0.9 ml, 15.54 mmol) and 1,3,5-triazine (840 mg, 10.36 mmol) is added to a solution of (2S,6RS)-4-(3-amino-4-cyano-benzyl)-2,6-dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl ester (2.03 g, 5.18 mmol) in ethanol. The resulting mixture is heated to reflux overnight. Replaced the ethanol with ethyl acetate and washed with saturated sodium bicarbonate (5 mL). The ethyl acetate layer is dried with magnesium sulfate, filtered and condensed. The resulting residue is purified by flash colunm (SiO2, 20% methanol/methylene chloride) to give the product (2S,6RS)-4-(4-amino-quinazolin-7-ylmethyl)-2,6-dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl ester (1.85 g, 85%) as a yellow solid. C23H25N5O3 MS m/z: 420.
Workup
- temperatureThe resulting mixture is heated
- temperatureto reflux overnight
- washwashed with saturated sodium bicarbonate (5 mL)
- dry with materialThe ethyl acetate layer is dried with magnesium sulfate
- filtrationfiltered
- customcondensed
- customThe resulting residue is purified by flash colunm (SiO2, 20% methanol/methylene chloride)
Sources & evidence
- ORD record
- ord-5d393f2a70f241ca989619526d6e0e9f
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07612075B2
Reaction notes
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