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

Sodium hydride → 5-(6,7,8,9-Tetrahydro-5H-pyrido[2,3-b]azepin-2-yl)-pentanoic acid methylamide

HRID 2187386
노트
인쇄 미리보기

반응식

HRID 2187386 반응식
[CH3:1][NH:2][C:3](=[O:19])[CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][CH2:17][NH2:18])=[CH:10][N:9]=1.[H-].[Na+]>>[CH3:1][NH:2][C:3](=[O:19])[CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]2[CH2:14][CH2:15][CH2:16][CH2:17][NH:18][C:10]=2[N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24758Sodium hydrideHCID 220826725-[5-(4-Aminobutyl)pyridin-2-YL]-N-methylpentanamide

생성물 1

HCID 220826735-(6,7,8,9-Tetrahydro-5H-pyrido[2,3-b]azepin-2-yl)-pentanoic acid methylamide

실험 절차

A mixture of 11-7 (24 g, 91.2 mmol) and NaH (10.9 g of a 60% weight dispersion in mineral oil, 273 mmol) in xylenes (500 mL) was purged with argon for 30 min, and then heated at reflux for 72 hours. The mixture was cooled, quenched with ethanol, diluted with 10% aqueous potassium carbonate and extracted with ethyl acetate. The organics were dried over MgSO4, and concentrated to an oil. The residue was chromatographed on silica gel (70:25:5 CHCl3/EtOAc/MeOH/H2O) to give 11-8 as a white solid.

후처리

  1. customwas purged with argon for 30 min
  2. temperatureheated
  3. temperatureat reflux for 72 hours
  • temperatureThe mixture was cooled
  • customquenched with ethanol
  • additiondiluted with 10% aqueous potassium carbonate
  • extractionextracted with ethyl acetate
  • dry with materialThe organics were dried over MgSO4
  • concentrationconcentrated to an oil
  • customThe residue was chromatographed on silica gel (70:25:5 CHCl3/EtOAc/MeOH/H2O)
  • 출처 및 근거

    ORD 기록
    ord-9fe5baa1f4e44925b48ac668b03ff758
    출처 데이터셋
    uspto-grants-2002_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06410526B1

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트