Sodium Hydroxide → HCID 131716803, compound

HRID 982507Notes

Reaction equation

HRID 982507 reaction equation
C1(N)C(F)=C(F)C(F)=C([NH2:10])C=1F.Cl.Cl.[CH3:15][N:16]1[CH2:21][CH2:20][C:19](=[C:22]2[C:28]3[CH:29]=[C:30]([CH2:33]N)[CH:31]=[CH:32][C:27]=3[CH:26]=[CH:25][C:24]3[CH:35]=[CH:36][CH:37]=[CH:38][C:23]2=3)[CH2:18][CH2:17]1.CO[C:41]1[CH:42]=[C:43]([CH:47]=[C:48](OC)[C:49]=1OC)[C:44](Cl)=[O:45].[OH-].[Na+]>C1(C)C=CC=CC=1>[CH3:15][N:16]1[CH2:17][CH2:18][C:19](=[C:22]2[C:28]3[CH:29]=[C:30]([CH2:33][C:47]4[CH:48]=[CH:49][CH:41]=[CH:42][C:43]=4[C:44]([NH2:10])=[O:45])[CH:31]=[CH:32][C:27]=3[CH:26]=[CH:25][C:24]3[CH:35]=[CH:36][CH:37]=[CH:38][C:23]2=3)[CH2:20][CH2:21]1

Participants

6

Procedure

To a mixture of 0.50 g (1.26 mmol) of the dihydrochloride salt of 1-methyl-4-(3-aminomethyl-5H-dibenzo[a,d]cycloheptene-5-ylidene)piperidine and 0.25 g (1.08 mmol) 3,4,5-trimethoxybenzoyl chloride in 25 ml of toluene was added 1 ml of 10% aqueous sodium hydroxide. The mixture was shaken vigorously for 5 minutes. The toluene was removed by evaporation under reduced pressure and the residual gum was redissolved in chloroform. This chloroform phase was separated, dried over magnesium sulfate, filtered, and the chloroform was removed by evaporation. The crystalline residue was recrystallized from acetonitrile to give 3,4,5-trimethoxy-N-((5-(1-methyl-4-piperidinylidene)-5H-dibenzo[a,d]cyclohepten-3-yl)methylbenzamide, mp 200°-202° C.

Workup

  1. customThe toluene was removed by evaporation under reduced pressure
  2. dissolutionthe residual gum was redissolved in chloroform
  3. customThis chloroform phase was separated
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customthe chloroform was removed by evaporation
  7. customThe crystalline residue was recrystallized from acetonitrile

Sources & evidence

ORD record
ord-c82ee5e07de64e1aa070d101a8a2142d
Source dataset
uspto-grants-1991_02
Patent number
US04996321

Reaction notes

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