Pyridine → HCID 86744410, 화합물

HRID 1111031노트

반응식

HRID 1111031 반응식
[N-:1]=[C:2]=[O:3].[CH2:4]([O:7][C:8](=[O:12])[C@H:9]([CH3:11])[NH2:10])[CH:5]=[CH2:6].[N:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.Cl.N[OH:21].C(OC)(OC)OC.[CH2:29]1COC[CH2:30]1>CO>[OH:21][N:13]=[CH:18][C:17]1[CH:30]=[CH:29][C:14]([NH:1][C:2]([NH:10][CH:9]([C:8]([O:7][CH2:4][CH:5]=[CH2:6])=[O:12])[CH3:11])=[O:3])=[CH:15][CH:16]=1

참가 물질

7

반응물 5

HCID 1049PyridineHCID 8028Tetrahydrofuran2회HCID 9005Trimethyl orthoformateHCID 443297Hydroxyamine hydrochlorideHCID 86744409HCID 86744409, 화합물

생성물 1

HCID 86744410HCID 86744410, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 0.1 mol of p-aminobenzaldehyde ethylene glycol acetal in 100 mL of anhydrous THF is added dropwise over 10 minutes to a solution of 0.1 mol of alanine allyl ester isocyanate and 0.35 moI pyridine in 100 mL THF at room temperature under N2. The reaction mixture is stirred at room temperature for 2 hours. After 2 hours the solvent is removed by rotary evaporator. A solution of 0.11 mmol hydroxylamine hydrochloride and 0.1 mol trimethyl orthoformate in CH3OH is added, and the reaction mixture is heated to reflux under N2 for 1 hour. The reaction mixture is reduced to about 1/4 volume by rotary evaporator, and water is added. The product, N-[4-(hydroxyiminomethyl)phenyl]-N'-[1-(allyloxycarbonyl)ethyl]urea, is isolated by filtration and dried in vacuo.

후처리

  1. customAfter 2 hours the solvent is removed by rotary evaporator
  2. temperaturethe reaction mixture is heated
  3. temperatureto reflux under N2 for 1 hour
  4. customThe reaction mixture is reduced to about 1/4 volume by rotary evaporator, and water
  5. additionis added

출처 및 근거

ORD 기록
ord-e4a24f7162184dfb9a0af30802d641ac
출처 데이터셋
uspto-grants-1990_12
특허 번호
US04977272

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