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

2-Chlorobenzoxazole → 4-(2-Benzoxazolyl)hexahydro-1H-1,4-diazepine-1-ethanol

HRID 1780672
노트
인쇄 미리보기

반응식

HRID 1780672 반응식
[OH:1][CH2:2][CH2:3][N:4]1[CH2:10][CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1.Cl[C:12]1[O:13][C:14]2[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=2[N:16]=1>CN(C=O)C>[OH:1][CH2:2][CH2:3][N:4]1[CH2:10][CH2:9][CH2:8][N:7]([C:12]2[O:13][C:14]3[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=3[N:16]=2)[CH2:6][CH2:5]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 119862-ChlorobenzoxazoleHCID 27365502-(1,4-Diazepan-1-yl)ethan-1-ol

생성물 1

HCID 190472834-(2-Benzoxazolyl)hexahydro-1H-1,4-diazepine-1-ethanol수율 26.6%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A 2.329 g portion of homopiperazine dissolved in 10 ml of THF was mixed with 830 mg of iodoethyl alcohol to carry out 24 hours of reaction at room temperature. The reaction mixture was concentrated under a reduced pressure, and the resulting residue was purified by Sephadex LH-20 (Pharmacia) (chloroform:methanol=1:1) and Diaion HP-20 (Mitsubishi Chemicals) to obtain 305 mg of 1-(2-hydroxyethyl)homo-piperazine. Next, Under cooling with ice, 150 mg of 1-(2-hydroxyethyl)homopiperazine and 159 mg of 2-chlorobenzoxazole were added to 3 ml of DMF, and the reaction was carried out for 17 hours at the same temperature and then for 24 hours at room temperature. The reaction mixture was concentrated under a reduced pressure, and the resulting residue was dissolved in 100 ml of ethyl acetate, washed with sodium hydrogencarbonate aqueous solution (pH 8) and water in that order, dehydrated with sodium sulfate and then concentrated under a reduced pressure. Thereafter, the resulting residue was purified by a silica gel column chromatography (chloroform:methanol=30:1) to obtain 72 mg of the title compound.

후처리

  1. waitfor 24 hours at room temperature
  2. concentrationThe reaction mixture was concentrated under a reduced pressure
  3. dissolutionthe resulting residue was dissolved in 100 ml of ethyl acetate
  4. washwashed with sodium hydrogencarbonate aqueous solution (pH 8) and water in that order
  5. concentrationconcentrated under a reduced pressure
  6. customThereafter, the resulting residue was purified by a silica gel column chromatography (chloroform:methanol=30:1)

출처 및 근거

ORD 기록
ord-bc5da25555fc4763bd56a9c7721645cd
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05631257

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트