p-Aminoacetophenone → HCID 86742139, compound

HRID 649690Notes

Reaction equation

HRID 649690 reaction equation
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[CH:6][CH:5]=1)=O.[N-:11]=[C:12]=[O:13].[CH3:14][O:15][C:16](=[O:30])[C@H:17]([CH2:19][C:20]1[CH:25]=[CH:24][C:23]([O:26][C:27](=[O:29])[CH3:28])=[CH:22][CH:21]=1)N.Cl.[NH2:32][OH:33].C(OC)(OC)OC>C1COCC1.N1C=CC=CC=1>[OH:33][N:32]=[C:2]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:12]([NH:11][CH:17]([C:16]([O:15][CH3:14])=[O:30])[CH2:19][C:20]2[CH:25]=[CH:24][C:23]([O:26][C:27](=[O:29])[CH3:28])=[CH:22][CH:21]=2)=[O:13])=[CH:6][CH:5]=1)[CH3:1]

Participants

7

Procedure

A solution of 2.7 g 4-aminoacetophenone in 40 mL is THF is dropwise to a solution of 0.02 mol of O-acetyltyrosine methyl ester isocyanate and 5 mL pyridine in 40 mL THF, and the reaction mixture is stirred for 3 hours. The solvent is then removed by rotary evaporator. The residue is dispersed in 50 mL CH3OH, and 0.022 mol hydroxylamine hydrochloride and 0.06 mol trimethyl orthoformate are added. The reaction mixture is heated to reflux for 10 hours. The solvent is removed by rotary evaporator. Addition of water to the residue results in precipitation of N-[4-(1-hydroxyiminoethyl)phenyl]-N'-[1-methoxycarbonyl-2-(4-acetyloxyphenyl)ethyl]urea, which is isolated by filtration and dried.

Workup

  1. customThe solvent is then removed by rotary evaporator
  2. additionThe residue is dispersed in 50 mL CH3OH
  3. temperatureThe reaction mixture is heated
  4. temperatureto reflux for 10 hours
  5. customThe solvent is removed by rotary evaporator
  6. additionAddition of water to the residue

Sources & evidence

ORD record
ord-20c24fe767b54b09bfeba88201b49b3b
Source dataset
uspto-grants-1988_04
Patent number
US04740611

Reaction notes

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