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

1,4-Dioxane → 5-(4-Chloro-phenyl)-6-cyclobutoxy-pyridin-3-ylamine

HRID 1958194
노트
인쇄 미리보기

반응식

HRID 1958194 반응식
C(OC(=O)[NH:7][C:8]1[CH:9]=[N:10][C:11]([O:21][CH:22]2[CH2:25][CH2:24][CH2:23]2)=[C:12]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=2)[CH:13]=1)(C)(C)C.O1CCOCC1>Cl>[Cl:20][C:17]1[CH:18]=[CH:19][C:14]([C:12]2[CH:13]=[C:8]([NH2:7])[CH:9]=[N:10][C:11]=2[O:21][CH:22]2[CH2:25][CH2:24][CH2:23]2)=[CH:15][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 312751,4-DioxaneHCID 68071757[5-(4-Chloro-phenyl)-6-cyclobutoxy-pyridin-3-yl]-carbamic acid tert-butyl ester

생성물 1

HCID 672811445-(4-Chloro-phenyl)-6-cyclobutoxy-pyridin-3-ylamine수율 46.9%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

[5-(4-Chloro-phenyl)-6-cyclobutoxy-pyridin-3-yl]-carbamic acid tert-butyl ester (1.042 g, 2.78 mmol) was dissolved in 4M HCl in dioxane (10.4 ml, 41.7 mmol). The reaction mixture was a light yellow solution and was stirred at room temperature for 1 h. The mixture was partitioned between ethyl acetate and 1M Na2CO3 solution. The organic phases were combined, dried with MgSO4 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 100 g, 5% to 75% ethyl acetate in heptane) to give 0.358 g (46.9%) of the title compound as light red oil; LC-MS (UV peak area/ESI) 94.3%, 275.0950 (M+H)+.

후처리

  1. customThe mixture was partitioned between ethyl acetate and 1M Na2CO3 solution
  2. dry with materialdried with MgSO4
  3. concentrationconcentrated in vacuo
  4. customThe crude material was purified by flash chromatography (silica gel, 100 g, 5% to 75% ethyl acetate in heptane)

출처 및 근거

ORD 기록
ord-c846f2c4743045c18923962498ce0f75
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08410107B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트