Triethylamine → HCID 10113922, compound
Reaction equation
[C:1]([CH2:3][NH:4][C:5]([C:7]1([NH2:13])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1)=[O:6])#[N:2].Cl.[CH:15]1([N:20]2[CH2:25][CH2:24][CH:23]([C:26]3[CH:34]=[CH:33][C:29]([C:30](O)=[O:31])=[CH:28][CH:27]=3)[CH2:22][CH2:21]2)[CH2:19][CH2:18][CH2:17][CH2:16]1.C1C=CC2N(O)N=NC=2C=1.C(N(CC)CC)C>CN(C=O)C>[C:1]([CH2:3][NH:4][C:5]([C:7]1([NH:13][C:30](=[O:31])[C:29]2[CH:28]=[CH:27][C:26]([CH:23]3[CH2:22][CH2:21][N:20]([CH:15]4[CH2:19][CH2:18][CH2:17][CH2:16]4)[CH2:25][CH2:24]3)=[CH:34][CH:33]=2)[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1)=[O:6])#[N:2]Participants
6
Procedure
1-Amino-cyclohexanecarboxylic acid cyanomethyl-amide (0.74 mmol), 4-(1-cyclopentyl-piperidin-4-yl)-benzoic acid hydrochloride (0.74 mmol), HOBT (0.74 mmol), WSCD (0.74 mmol) and triethylamine (0.74 mmol) are dissolved in DMF (5 ml) and stirred overnight at rt. After evaporation of the solvent, the residue is dissolved in a mixture of water and sodium carbonate (to ensure basic conditions) and extracted three times with ethyl acetate. The combined extract is dried over sodium sulfate and evaporated. The residue is suspended in diethylether and the solid filtered of and dried (vacuum). A white powder with mp. 233-234° C., Rf=0.34 (CH2Cl2/MeOH (with 3N NH3)=9:1) is obtained.
Workup
- customAfter evaporation of the solvent
- dissolutionthe residue is dissolved in a mixture of water and sodium carbonate (to ensure basic conditions)
- extractionextracted three times with ethyl acetate
- extractionThe combined extract
- dry with materialis dried over sodium sulfate
- customevaporated
- filtrationthe solid filtered of and
- customdried (vacuum)
- customA white powder with mp. 233-234° C., Rf=0.34 (CH2Cl2/MeOH (with 3N NH3)=9:1) is obtained
Sources & evidence
- ORD record
- ord-05fd05d7f3eb47b9a057204c9ae5adef
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06642239B2
Reaction notes
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