홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Methanol → N-[(2,4-dichlorophenyl)methyl]-1,3,3-trimethyl-5-oxoprolinamide

HRID 2238549
노트
인쇄 미리보기

반응식

HRID 2238549 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH2:9][N+:10]#[C-:11].[CH3:12][C:13]([CH3:20])([CH:18]=O)[CH2:14][C:15](O)=[O:16].[CH3:21][NH2:22].C[OH:24]>>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH2:9][NH:10][C:11](=[O:24])[C@@H:18]1[C:13]([CH3:20])([CH3:12])[CH2:14][C:15](=[O:16])[N:22]1[CH3:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 887MethanolHCID 6329MethylamineHCID 27580712,4-Dichloro-1-(isocyanomethyl)benzeneHCID 247680973-Formyl-3-methylbutanoic acid

생성물 1

HCID 67460084N-[(2,4-dichlorophenyl)methyl]-1,3,3-trimethyl-5-oxoprolinamide

반응 조건

온도
100 °C

실험 절차

To a solution of (2,4-dichlorophenyl)methyl isocyanide (0.094 g, 0.5 mmol) and 3,3-dimethyl-4-oxobutanoic acid (0.065 mg, 0.5 mmol, prepared as described below) in methanol (2 ml) was added methylamine (0.080 ml, 33% solution in ethanol). The mixture was heated to 100° C. for 30 minutes in a microwave reactor. The solvent was removed in vacuo and the residue was purified by mass-directed automated HPLC to give a colourless gum which was triturated with diethyl ether to give N-[(2,4-dichlorophenyl)methyl]-1,3,3-trimethyl-5-oxoprolinamide (0.043 g) as a sticky white solid.

후처리

  1. customThe solvent was removed in vacuo
  2. customthe residue was purified
  3. customto give a colourless gum which
  4. customwas triturated with diethyl ether

출처 및 근거

ORD 기록
ord-7ad1baca3abb4612913e3b5f8a5b6451
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07718693B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트