1,2-Dichloroethane → HCID 57980110, compound
Reaction equation
[F:1][C:2]([F:19])([F:18])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([C:15]([OH:17])=O)=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.C(Cl)CCl.C1C=CC2N(O)N=NC=2C=1.CCN(C(C)C)C(C)C.[NH:43]1[CH2:47][CH2:46][CH2:45][C@H:44]1[CH2:48][N:49]1[CH2:53][CH2:52][CH2:51][CH2:50]1>ClCCl.CN(C=O)C.C(OCC)(=O)C.O>[N:49]1([CH2:48][C@@H:44]2[CH2:45][CH2:46][CH2:47][N:43]2[C:15]([C:12]2[CH:11]=[CH:10][C:9]([C:6]3[CH:5]=[CH:4][C:3]([C:2]([F:1])([F:19])[F:18])=[CH:8][CH:7]=3)=[CH:14][CH:13]=2)=[O:17])[CH2:53][CH2:52][CH2:51][CH2:50]1Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 4
Procedure
Procedure B′: 4′-Trifluoromethyl-biphenyl-4-carboxylic acid (2.7 g, 10.1 mmol) is suspended in dichloromethane (100 mL) and DMF (100 mL). EDC (2.33 g, 12.2 mmol) and HOBt (1.64 g, 12.2 mmol) were added at room temperature in that order. DIEA (4.4 mL, 25.3 mmol) and (S)(+)-1-(2-pyrrolidinylmethyl)pyrrolidine (1.56 g, 10.1 mmol) are added to the mixture. The mixture is stirred at room temperature for overnight. Water and ethyl acetate are added to the mixture. The aqueous layer is extracted with dichlormethane (2×), followed by ethyl acetate (2×). The combined organic layers are washed with brine (3×), dried over Na2SO4 and evaporated. The crude product is purified by silica-gel column chromatography (gradient: 100% CH2Cl2 to 10% 2M NH3 in MeOH/CH2Cl2) give the product. MS (ES+) 403.2
Workup
- extractionThe aqueous layer is extracted with dichlormethane (2×)
- washThe combined organic layers are washed with brine (3×)
- dry with materialdried over Na2SO4
- customevaporated
- customThe crude product is purified by silica-gel column chromatography (gradient: 100% CH2Cl2 to 10% 2M NH3 in MeOH/CH2Cl2)
- customgive the product
Sources & evidence
- ORD record
- ord-a2ccc647f074482d82b60ff88ddb3c84
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07632857B2
Reaction notes
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