Acetic Acid → HCID 13067121, compound

HRID 647632Notes

Reaction equation

HRID 647632 reaction equation
[Mn]([O-])(=O)(=O)=O.[K+].[Cl:7][C:8]1[CH:30]=[CH:29][C:11]2[C:12]3[C:13](=[C:24]([CH:27]=[O:28])[NH:25][CH:26]=3)[CH2:14][N:15]=[C:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[Cl:23])[C:10]=2[CH:9]=1.C(O)(=[O:33])C>CC(C)=O.S(=O)(O)[O-].[Na+]>[Cl:7][C:8]1[CH:30]=[CH:29][C:11]2[C:12]3[C:13](=[C:24]([C:27]([OH:33])=[O:28])[NH:25][CH:26]=3)[CH2:14][N:15]=[C:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[Cl:23])[C:10]=2[CH:9]=1

Participants

6

Procedure

A solution of 1.5 g (9.5 mmol) of potassium permanganate in 150 ml of 50% aqueous acetone was added dropwise to a solution of 1.6 g (4.5 mmol) of 8-chloro-6-(2-chlorophenyl)-2H,4H-pyrrolo[3,4-d][2]benzazepine-3-carboxaldehyde in 100 ml of acetone. After 2.5 hr the mixture was diluted with a saturated aqueous solution of sodium bisulfite, neutralized with the addition of acetic acid and extracted with methylene chloride. The methylene chloride solution was dried over anhydrous sodium sulfate and concentrated at reduced pressure to dryness. Trituration of the residue with methylene chloride gave yellow crystals, mp 216°-218°. Recrystallization from a mixture of ethanol and ether gave yellow prisms, mp 252°-254° (dec).

Workup

  1. extractionextracted with methylene chloride
  2. dry with materialThe methylene chloride solution was dried over anhydrous sodium sulfate
  3. concentrationconcentrated at reduced pressure to dryness
  4. customTrituration of the residue with methylene chloride gave yellow crystals, mp 216°-218°
  5. customRecrystallization
  6. additionfrom a mixture of ethanol and ether
  7. customgave yellow prisms, mp 252°-254° (dec)

Sources & evidence

ORD record
ord-7e1c52bf02b14195a3a0091ca74c45a0
Source dataset
uspto-grants-1983_10
Patent number
US04409390

Reaction notes

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