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

Cyclopropylamine → 3-Bromo-N-cyclopropylimidazo[1,2-a]pyrazin-8-amine

HRID 457010
노트
인쇄 미리보기

반응식

HRID 457010 반응식
[Br:1][C:2]1[N:6]2[C:7](Br)=[CH:8][N:9]=[CH:10][C:5]2=[N:4][CH:3]=1.[CH:12]1([NH2:15])[CH2:14][CH2:13]1.C(N(C(C)C)CC)(C)C>C1COCC1.C(Cl)Cl.O>[Br:1][C:2]1[N:6]2[CH:7]=[CH:8][N:9]=[C:10]([NH:15][CH:12]3[CH2:14][CH2:13]3)[C:5]2=[N:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 69828CyclopropylamineHCID 81531DiisopropylethylamineHCID 142075923,5-Dibromoimidazo[1,2-a]pyrazine

생성물 1

HCID 210709123-Bromo-N-cyclopropylimidazo[1,2-a]pyrazin-8-amine수율 14.5%

시약·촉매·용매 3

HCID 962Water용매HCID 6344Dichloromethane용매

반응 조건

온도
50 °C

실험 절차

To a solution of 3,5-dibromo-imidazo[1,2-a]pyrazine (D) (250 mg, 0.9 mmol) in THF (9 ml) was added cyclopropylamine (1.9 ml, 27 mmol) and diisopropylethylamine (DIPEA) (0.782 ml, 4.5 mmol). The mixture was heated at 50° C. in sealed tube overnight. The mixture was then cooled to rt, diluted with DCM and water. The organic layer was washed with brine, dried and concentrated. The residue was purified on a silica gel column to give 33 mg (yield 14.5%) of the title compound.

후처리

  1. temperatureThe mixture was then cooled to rt
  2. washThe organic layer was washed with brine
  3. customdried
  4. concentrationconcentrated
  5. customThe residue was purified on a silica gel column

출처 및 근거

ORD 기록
ord-cb98ee9cbba545a4be1c4c10b5f3a263
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07186832B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 8028
Tetrahydrofuran
용매