Hydrochloric Acid → HCID 20382243, compound

HRID 1973836Notes

Reaction equation

HRID 1973836 reaction equation
C(O)(=O)C(O)=O.[CH3:7][O:8][C:9]1[CH:10]=[C:11]([NH:15][C:16]2([C:30]([O:32]C)=[O:31])[CH2:21][CH2:20][N:19]([CH2:22][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[CH2:18][CH2:17]2)[CH:12]=[CH:13][CH:14]=1.[OH-].[K+].Cl.[OH-].[Na+]>O.C(O)CO>[CH3:7][O:8][C:9]1[CH:10]=[C:11]([NH:15][C:16]2([C:30]([OH:32])=[O:31])[CH2:17][CH2:18][N:19]([CH2:22][CH2:23][C:24]3[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=3)[CH2:20][CH2:21]2)[CH:12]=[CH:13][CH:14]=1

Participants

7

Procedure

A mixture of 39.5 parts of methyl 4-[N-(3-methoxyphenyl)amino]-1-(2-phenylethyl)-4-piperidinecarboxylate ethanedioate, 18 parts of potassium hydroxide and 90 parts of 1,2-ethanediol is stirred and refluxed for 3 hours. The reaction mixture is cooled to room temperature, poured onto 200 parts of water and acidified with a concentrated hydrochloric acid solution. The whole is strongly alkalized with a sodium hydroxide solution and stirred vigorously for one hour. The precipitated product is filtered off, dissolved in water and the solution is neutralized with acetic acid. The product is filtered off and crystallized from N,N-dimethylformamide, yielding 27.4 parts (72.3%) of 4-[(3-methoxyphenyl)amino]-1-(2-phenylethyl)-4-piperidinecarboxylic acid; mp. 265.1° C.

Workup

  1. temperaturerefluxed for 3 hours
  2. stirringstirred vigorously for one hour
  3. filtrationThe precipitated product is filtered off
  4. dissolutiondissolved in water
  5. filtrationThe product is filtered off
  6. customcrystallized from N,N-dimethylformamide

Sources & evidence

ORD record
ord-8e02b93bd82b43f893a7806e15a09f5b
Source dataset
uspto-grants-1976_12
Patent number
US03998834

Reaction notes

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