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

5-Bromo-1-methyl-1H-tetrazole → 1-[(1-Methyl-1H-tetrazol-5-yl)amino]-3-[3-(1-piperidinylmethyl)phenoxy]-2-propanol

HRID 2164743
노트
인쇄 미리보기

반응식

HRID 2164743 반응식
[NH2:1][CH2:2][CH:3]([OH:19])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH2:12][N:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]2)[CH:7]=1.Br[C:21]1[N:25]([CH3:26])[N:24]=[N:23][N:22]=1>C(O)C>[CH3:26][N:25]1[C:21]([NH:1][CH2:2][CH:3]([OH:19])[CH2:4][O:5][C:6]2[CH:11]=[CH:10][CH:9]=[C:8]([CH2:12][N:13]3[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]3)[CH:7]=2)=[N:22][N:23]=[N:24]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 127974465-Bromo-1-methyl-1H-tetrazoleHCID 131898251-Amino-3-{3-[(piperidin-1-yl)methyl]phenoxy}propan-2-ol

생성물 1

HCID 204032041-[(1-Methyl-1H-tetrazol-5-yl)amino]-3-[3-(1-piperidinylmethyl)phenoxy]-2-propanol수율 53.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 1-amino-3-[3-(1-piperidinylmethyl)phenoxy]-2-propanol (1.19 g) and 5-bromo-1-methyl-1H-tetrazole (0.735 g) in absolute ethanol (6 ml) was heated in an autoclave at 125° for 18 h. The mixture was cooled, evaporated, saturated with sodium carbonate solution (30 ml) and ethyl acetate (30 ml) added. The mixture was stirred for 15 min. and filtered to give a white solid (830 mg) which was recrystallised from ethyl acetate (20 ml) to give the title compound (0.58 g) as white micro-crystals, m.p. 156°-7°.

후처리

  1. temperatureThe mixture was cooled
  2. customevaporated, saturated with sodium carbonate solution (30 ml) and ethyl acetate (30 ml)
  3. additionadded
  4. filtrationfiltered

출처 및 근거

ORD 기록
ord-ba99234dedfd4f1b9b7b351074361312
출처 데이터셋
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04507296

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트