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Isopropyl isocyanate → HCID 86617475, 화합물

HRID 1162825
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HRID 1162825 반응식
[F:1][C:2]1[CH:21]=[CH:20][C:5]([CH2:6][N:7]2[CH2:12][CH:11]([CH2:13][CH2:14][N:15]([O:17][CH3:18])[CH3:16])[NH:10][CH2:9][C:8]2=[O:19])=[CH:4][CH:3]=1.[CH:22]([N:25]=[C:26]=[O:27])([CH3:24])[CH3:23]>C(Cl)Cl>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][N:7]2[C:8](=[O:19])[CH2:9][N:10]([C:26]([NH:25][CH:22]([CH3:24])[CH3:23])=[O:27])[CH:11]([CH2:13][CH2:14][N:15]([O:17][CH3:18])[CH3:16])[CH2:12]2)=[CH:20][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 61277Isopropyl isocyanateHCID 588579491-[(4-Fluorophenyl)methyl]-5-[2-(methoxymethylamino)ethyl]-2-piperazinone

생성물 1

HCID 86617475HCID 86617475, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 1-(4-fluorobenzyl)-5-{2-[methoxy(methyl)amino]ethyl}piperazine-2-one (784 mg, 2.65 mmol) in anhydrous CH2Cl2 (13 mL) was treated with isopropyl isocyanate (391 μL, 3.98 mmol) and stirred under inert atmosphere at ambient temperature for 18 h. The solvent was removed in vacuo, and the resulting oil was purified by silica gel chromatography (EtOAc to 5% MeOH/EtOAc to 10% MeOH/EtOAc) to afford the title urea as a light orange oil.

후처리

  1. customThe solvent was removed in vacuo
  2. customthe resulting oil was purified by silica gel chromatography (EtOAc to 5% MeOH/EtOAc to 10% MeOH/EtOAc)

출처 및 근거

ORD 기록
ord-d348f2bf3cc94658b9fbf8751398fca9
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07820680B2

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