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

HCID 22020948, 화합물 → HCID 22020967, 화합물

HRID 1793336
노트
인쇄 미리보기

반응식

HRID 1793336 반응식
CS(O[CH2:6][CH:7]1[O:15][C:10]2=[N:11][CH:12]=[CH:13][CH:14]=[C:9]2[O:8]1)(=O)=O.[NH2:16][CH2:17][CH2:18][CH2:19][N:20]1[CH2:25][C:24]([CH3:27])([CH3:26])[CH2:23][NH:22][C:21]1=[O:28]>>[O:8]1[C:9]2[C:10](=[N:11][CH:12]=[CH:13][CH:14]=2)[O:15][CH:7]1[CH2:6][NH:16][CH2:17][CH2:18][CH2:19][N:20]1[CH2:25][C:24]([CH3:26])([CH3:27])[CH2:23][NH:22][C:21]1=[O:28]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 22020948HCID 22020948, 화합물HCID 22020971HCID 22020971, 화합물

생성물 1

HCID 22020967HCID 22020967, 화합물수율 50.2%

반응 조건

온도
100 °C

실험 절차

A mixture of intermediate (6) (0.0092 mol) and intermediate (13) (0.0183 mol) was stirred for 2 hours at 100° C. The crude reaction mixture was purified by open column chromatography over silica gel (eluent: CH2Cl2/CH3OH 90/10). The desired fractions were collected and the solvent was evaporated. The residue was washed with DIPE, then dried, yielding 1.48 g of (±)-1-[3-[(1,3-dioxolo[4,5-b]pyridin-2-ylmethyl)amino]-propyl]tetrahydro-5,5-dimethyl-2(1H)-pyrimidinone (compound 10).

후처리

  1. customThe crude reaction mixture
  2. custom
was purified by open column chromatography over silica gel (eluent: CH2Cl2/CH3OH 90/10)
  • customThe desired fractions were collected
  • customthe solvent was evaporated
  • washThe residue was washed with DIPE
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-b9164710d6a9432fba83d9bfa12c024f
    출처 데이터셋
    uspto-grants-2006_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07081453B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트