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

Tetrahydrofuran → 4-Fluoro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide

HRID 1589182
노트
인쇄 미리보기

반응식

HRID 1589182 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=O)=[CH:4][CH:3]=1.C(N1C=CN=C1)(N1C=CN=C1)=O.O1CCCC1.Cl.Cl.[N:31]1([CH2:36][CH2:37][CH2:38][NH2:39])[CH:35]=[CH:34][N:33]=[CH:32]1>O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([NH:39][CH2:38][CH2:37][CH2:36][N:31]2[CH:35]=[CH:34][N:33]=[CH:32]2)=[O:11])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8028TetrahydrofuranHCID 98372-(4-Fluorophenyl)acetic acidHCID 682631,1'-CarbonyldiimidazoleHCID 122509693-(Imidazole-1-yl)-propylamine Dihydrochloride

생성물 1

HCID 135889554-Fluoro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide

시약·촉매·용매 1

HCID 962Water
용매

실험 절차

A mixture of 1.54 g. of 4-fluorophenylacetic acid, 1.62 g. of 1,1'-carbonyldiimidazole and 30 ml. of tetrahydrofuran was stirred for 2 hours, then 1.98 g. of 1H-imidazole-1-propanamine dihydrochloride was added. Stirring was continued at room temperature for an additional 18 hours, then at reflux temperature for 5 hours, 5 ml. of water was added, the mixture was heated for 30 minutes and then concentrated to remove the volatile material. The residue was diluted with methylene chloride and 25 ml. of 1N sodium hydroxide and the layers separated. The organic layer was washed with water, dried over magnesium sulfate and concentrated, giving the desired product as a viscous oil.

후처리

  1. additionA mixture of 1.54 g
  2. temperatureat reflux temperature for 5 hours
  3. temperaturethe mixture was heated for 30 minutes
  4. concentrationconcentrated
  5. customto remove the volatile material
  6. additionThe residue was diluted with methylene chloride and 25 ml
  7. customof 1N sodium hydroxide and the layers separated
  8. washThe organic layer was washed with water
  9. dry with materialdried over magnesium sulfate
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-10943a0c07ab4282b49f50323488230c
출처 데이터셋
uspto-grants-1986_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04568687

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트