p-Aminoacetophenone → HCID 86741882, 화합물

HRID 649689노트

반응식

HRID 649689 반응식
[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:24])[C@H:17]([CH2:19][S:20][C:21](=[O:23])[CH3:22])N.Cl.[NH2:26][OH:27].C(OC)(OC)OC>C1COCC1.N1C=CC=CC=1>[OH:27][N:26]=[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:24])[CH2:19][S:20][C:21](=[O:23])[CH3:22])=[O:13])=[CH:6][CH:5]=1)[CH3:1]

참가 물질

7

반응물 4

HCID 7468p-AminoacetophenoneHCID 9005Trimethyl orthoformateHCID 443297Hydroxyamine hydrochlorideHCID 86741874HCID 86741874, 화합물

생성물 1

HCID 86741882HCID 86741882, 화합물

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 2.7 g 4-aminoacetophenone in 40 mL THF is added dropwise to a solution of 0.02 mol of S-acetylcysteine 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-(acetylthio)ethyl]urea, which is isolated by filtration and dried.

후처리

  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

출처 및 근거

ORD 기록
ord-a5828d53eeea46d7a180d36272f53566
출처 데이터셋
uspto-grants-1988_04
특허 번호
US04740611

반응 노트

불러오는 중…