Water → N-[4-[3-(1-adamantyl)-4-methoxy benzamido]-benzoyl]pyrrolidine

HRID 1651324Notes

Reaction equation

HRID 1651324 reaction equation
[NH2:1][C:2]1[CH:14]=[CH:13][C:5]([C:6]([N:8]2[CH2:12][CH2:11][CH2:10][CH2:9]2)=[O:7])=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:22]12([C:32]3[CH:33]=[C:34]([CH:38]=[CH:39][C:40]=3[O:41][CH3:42])[C:35](Cl)=[O:36])[CH2:31][CH:26]3[CH2:27][CH:28]([CH2:30][CH:24]([CH2:25]3)[CH2:23]1)[CH2:29]2.O>ClCCl>[C:22]12([C:32]3[CH:33]=[C:34]([CH:38]=[CH:39][C:40]=3[O:41][CH3:42])[C:35]([NH:1][C:2]3[CH:3]=[CH:4][C:5]([C:6]([N:8]4[CH2:9][CH2:10][CH2:11][CH2:12]4)=[O:7])=[CH:13][CH:14]=3)=[O:36])[CH2:23][CH:24]3[CH2:30][CH:28]([CH2:27][CH:26]([CH2:25]3)[CH2:31]1)[CH2:29]2

Participants

6

Procedure

1.7 g (9 mmoles) of N-p-aminobenzoyl pyrrolidine and 1 g (10 mmoles) of triethylamine are dissolved in 30 ml of dichloromethane. With stirring, 2.8 g (9 mmoles) of 3-(1-adamantyl)-4-methoxybenzoyl chloride dissolved in 60 ml of dichloromethane are added. The reaction mixture is stirred for 16 hours, at which point water is added and the reaction mixture is extracted with dichloromethane. The extract is washed with water, extracted with methylene chloride and dried on MgSO4. The solvents are evaporated and the residue (yellow foam) is crystallized in ethyl acetate to give 3.0 g (73% yield) of N-[4-[3-(1-adamantyl)-4-methoxy benzamido]-benzoyl]pyrrolidine which melts at 239°-242° C.

Workup

  1. additionare added
  2. stirringThe reaction mixture is stirred for 16 hours, at which
  3. additionis added
  4. extractionthe reaction mixture is extracted with dichloromethane
  5. washThe extract is washed with water
  6. extractionextracted with methylene chloride
  7. customdried on MgSO4
  8. customThe solvents are evaporated
  9. customthe residue (yellow foam) is crystallized in ethyl acetate

Sources & evidence

ORD record
ord-7318a310c1334f2eb5674b86b3648d85
Source dataset
uspto-grants-1990_05
Patent number
US04927928

Reaction notes

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