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1,2-Dichloroethane → (+/-)2-Chloro-N-[2-methyl-2-(2-methyl-1-pyrrolidinyl)-1-phenylpropyl]-3-(trifluoromethyl)benzamide

HRID 20840
Notes
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Reaction equation

HRID 20840 reaction equation
[CH3:1][C:2]([N:12]1[CH2:16][CH2:15][CH2:14][CH:13]1[CH3:17])([CH3:11])[CH:3]([NH2:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Cl:18][C:19]1[C:27]([C:28]([F:31])([F:30])[F:29])=[CH:26][CH:25]=[CH:24][C:20]=1[C:21](O)=[O:22].C(Cl)CCl.C1C=CC2N(O)N=NC=2C=1.C(=O)([O-])O.[Na+]>C(Cl)Cl>[Cl:18][C:19]1[C:27]([C:28]([F:29])([F:30])[F:31])=[CH:26][CH:25]=[CH:24][C:20]=1[C:21]([NH:10][CH:3]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:2]([CH3:1])([N:12]1[CH2:16][CH2:15][CH2:14][CH:13]1[CH3:17])[CH3:11])=[O:22]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 111,2-DichloroethaneHCID 757711-HydroxybenzotriazoleHCID 516892Sodium BicarbonateHCID 27366772-Chloro-3-(trifluoromethyl)benzoic acidHCID 59347786[2-Methyl-2-(2-methyl-1-pyrrolidinyl)-1-phenylpropyl]amine

Product 1

HCID 59347881
(+/-)2-Chloro-N-[2-methyl-2-(2-methyl-1-pyrrolidinyl)-1-phenylpropyl]-3-(trifluoromethyl)benzamide

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A mixture of [2-methyl-2-(2-methyl-1-pyrrolidinyl)-1-phenylpropyl]amine D26 (0.150 g; 0.647 mmol), 2-chloro-3-(trifluoromethyl)benzoic acid (0.174 g; 0.775 mmol), EDC (0.149 g; 0.777 mmol) and HOBt (0.020 g; 0.148 mmol) in DCM (4 ml) was shaken at room temperature for 66 hours. Saturated sodium hydrogen carbonate (8 ml) was added and shaking continued for 0.5 hours. The organic layer was passed through a phase separation cartridge and applied to a 2 g SCX column. The column was washed with DCM and methanol and the product eluted with 1M ammonia in methanol. The crude product was purified by chromatography on silica gel (20 g) eluting with 0-100% ethyl acetate in pentane gradient to afford the title compound as two pairs of enantiomers.

Workup

  1. stirringshaking
  2. waitcontinued for 0.5 hours
  3. customThe organic layer was passed through a phase separation cartridge
  4. washThe column was washed with DCM and methanol
  5. washthe product eluted with 1M ammonia in methanol
  6. customThe crude product was purified by chromatography on silica gel (20 g)
  7. washeluting with 0-100% ethyl acetate in pentane gradient

Sources & evidence

ORD record
ord-d442d140b910474784016bfda8a268a9
Source dataset
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07745642B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes