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

2-Chlorobenzoxazole → N-(4-(3-Bromopyridin-2-yloxy)phenyl)benzo[D]oxazol-2-amine

HRID 1880086
노트
인쇄 미리보기

반응식

HRID 1880086 반응식
[Br:1][C:2]1[C:3]([O:8][C:9]2[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=2)=[N:4][CH:5]=[CH:6][CH:7]=1.Cl[C:17]1[O:18][C:19]2[CH:25]=[CH:24][CH:23]=[CH:22][C:20]=2[N:21]=1>CN1C(=O)CCC1>[Br:1][C:2]1[C:3]([O:8][C:9]2[CH:15]=[CH:14][C:12]([NH:13][C:17]3[O:18][C:19]4[CH:25]=[CH:24][CH:23]=[CH:22][C:20]=4[N:21]=3)=[CH:11][CH:10]=2)=[N:4][CH:5]=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 119862-ChlorobenzoxazoleHCID 577562564-(3-Bromopyridin-2-yloxy)benzenamine

생성물 1

HCID 59327040N-(4-(3-Bromopyridin-2-yloxy)phenyl)benzo[D]oxazol-2-amine

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매

반응 조건

온도
170 °C

실험 절차

A mixture of 4-(3-bromopyridin-2-yloxy)aniline (1.73 g, 6.53 mmol) and 2-chlorobenzoxazole (1.00 g, 6.51 mmol, TCI America) in NMP (3 mL) was sealed in a screw-cap flask and heated at 170° C. for 20 h. The reaction was cooled to rt and partitioned with water/EtOAc. The aqueous layer was extracted with EtOAc (3×) and the combined organic layers were evaporated onto silica gel and purified by flash chromatography (Isco (80 gram)) eluting with EtOAc:hexanes (0:1→1:2) a tan amorphous solid. MS (ESI, pos. ion) m/z: 382.0, 383.9 (M+1).

후처리

  1. customwas sealed in a screw-cap flask
  2. temperatureThe reaction was cooled to rt
  3. custompartitioned with water/EtOAc
  4. extractionThe aqueous layer was extracted with EtOAc (3×)
  5. customthe combined organic layers were evaporated onto silica gel
  6. custompurified by flash chromatography (Isco (80 gram))
  7. washeluting with EtOAc:hexanes (0:1→1:2) a tan amorphous solid

출처 및 근거

ORD 기록
ord-e09e6e44fc394d7e9912e641b6d3d8ab
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318718B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트