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

Tetrahydrofuran → 6-(2-Amino-4-pyrimidinyl)-4-(methyloxy)-1H-indazol-3-amine

HRID 2367203
노트
인쇄 미리보기

반응식

HRID 2367203 반응식
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[CH:15]=[C:14](OC)[C:11]([C:12]#[N:13])=[C:10](F)[CH:9]=2)[CH:5]=[CH:4][N:3]=1.[OH2:19].[NH2:20][NH2:21].[CH2:22]1COCC1>>[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[CH:15]=[C:14]3[C:11]([C:12]([NH2:13])=[N:20][NH:21]3)=[C:10]([O:19][CH3:22])[CH:9]=2)[CH:5]=[CH:4][N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 8028TetrahydrofuranHCID 24654Hydrazine hydrate (1:1)HCID 585044614-(2-Amino-4-pyrimidinyl)-2-fluoro-6-(methyloxy)benzonitrile

생성물 1

HCID 462143136-(2-Amino-4-pyrimidinyl)-4-(methyloxy)-1H-indazol-3-amine수율 49%

반응 조건

온도
90 °C

실험 절차

To a slurry of 4-(2-amino-4-pyrimidinyl)-2-fluoro-6-(methyloxy)benzonitrile (0.20 g, 0.82 mmol) in THF (2 mL) was added hydrazine monohydrate (1.3 mL), and the resulting mixture was stirred at 90° C. until the starting material was consumed as judged by LCMS (˜12 hours). The reaction mixture was concentrated to afford the title compound (102 mg, 49%) as a bright yellow solid. LC-MS (ES) m/z=257 [M+H]+. 1H NMR (400 MHz, DMSO-d6): δ 3.94 (s, 3H), 5.06 (s, 2H), 6.65 (s, 2H), 6.97 (s, 1H), 7.16 (d, J=5.3 Hz, 1H), 7.54 (d, J=1.0 Hz, 1H), 8.30 (d, J=5.3 Hz, 1H), 11.67 (bs, 1H).

후처리

  1. customwas consumed
  2. customas judged by LCMS (˜12 hours)
  3. concentrationThe reaction mixture was concentrated

출처 및 근거

ORD 기록
ord-2142675385534c5595f02d8b6926d28d
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08697685B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트