Carbonic acid-guanidine (1:1) → HCID 13225512, compound

HRID 464186Notes

Reaction equation

HRID 464186 reaction equation
C(=O)(O)O.[NH2:5][C:6]([NH2:8])=[NH:7].C[O-].[Na+].[Cl:12][C:13]1[CH:36]=[CH:35][C:16]2[C:17](=O)[C:18](=[CH:30]N(C)C)[CH2:19][N+:20]([O-:29])=[C:21]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[F:28])[C:15]=2[CH:14]=1>CO.O>[NH2:7][C:6]1[N:8]=[CH:30][C:18]2[CH2:19][N+:20]([O-:29])=[C:21]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[F:28])[C:15]3[CH:14]=[C:13]([Cl:12])[CH:36]=[CH:35][C:16]=3[C:17]=2[N:5]=1

Participants

6

Procedure

In two equal portions 28 g (150 mmole) of guanidine carbonate and 38 ml (150 mmole) of a 4.09M methanol solution of sodium methoxide was added over a 2 hr period to a solution of 7.0 g (20 mmole) of 8-chloro-1-(2-fluorophenyl)-3,4-dihydro-4-[(dimethylamino)methylene]-5H-2-benzazepin-5-one-2-oxide in 210 ml of methanol. The mixure was diluted with water and extracted with methylene chloride. The methylene chloride solution was dried over anhydrous sodium sulfate and concentrated at reduced pressure to give a red solid. Recrystallization from a mixture of methanol and ethyl acetate gave the product as fine yellow needles, m.p. 320°-323° C.

Workup

  1. extractionextracted with methylene chloride
  2. dry with materialThe methylene chloride solution was dried over anhydrous sodium sulfate
  3. concentrationconcentrated at reduced pressure
  4. customto give a red solid
  5. customRecrystallization
  6. additionfrom a mixture of methanol and ethyl acetate

Sources & evidence

ORD record
ord-2e49315dce194d7480246aee89d636a0
Source dataset
uspto-grants-1985_10
Patent number
US04546183

Reaction notes

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