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

Potassium Carbonate → 1-(4-Ethynyl-3-methoxyphenyl)-4-methylpiperazine

HRID 1403209
노트
인쇄 미리보기

반응식

HRID 1403209 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([N:15]2[CH2:20][CH2:19][N:18]([CH3:21])[CH2:17][CH2:16]2)[CH:6]=[CH:7][C:8]=1[C:9]#[C:10][Si](C)(C)C.C(=O)([O-])[O-].[K+].[K+]>CO>[C:9]([C:8]1[CH:7]=[CH:6][C:5]([N:15]2[CH2:16][CH2:17][N:18]([CH3:21])[CH2:19][CH2:20]2)=[CH:4][C:3]=1[O:2][CH3:1])#[CH:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 867252923-Methoxy-4-[(trimethylsilyl)ethynyl]phenyl-4-methylpiperazine

생성물 1

HCID 712395881-(4-Ethynyl-3-methoxyphenyl)-4-methylpiperazine수율 84.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 1-{3-methoxy-4-[(trimethylsilyl)ethynyl]phenyl-4-methylpiperazine (583 mg, 1.927 mmol) in anhydrous methanol (12 mL) is treated with powdered anhydrous potassium carbonate under stirring at room temperature for 1.5 h. After removing the solvent under vacuum the residue was taken up with EtOAc (80 mL) and water (5 mL). The phases were separated, the organic phase was washed with brine (3×10 mL), water (10 mL), dried over sodium sulfate and the solvent removed under vacuum. The dark oil obtained was purified by chromatography on silica gel (DCM/MeOH/TEA 90/10/0.1) to give the title compound as brownish solid (374 mg, 84.2%).

후처리

  1. customAfter removing the solvent under vacuum the residue
  2. customThe phases were separated
  3. washthe organic phase was washed with brine (3×10 mL), water (10 mL)
  4. dry with materialdried over sodium sulfate
  5. customthe solvent removed under vacuum
  6. customThe dark oil obtained
  7. customwas purified by chromatography on silica gel (DCM/MeOH/TEA 90/10/0.1)

출처 및 근거

ORD 기록
ord-a062148cf68948158b9cfee5bdb75259
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08912200B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트