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

1H-Indazole-6-carbaldehyde → 1-(1H-Indazol-6-yl)ethanol

HRID 1615257
노트
인쇄 미리보기

반응식

HRID 1615257 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH:10]=[O:11])[CH:8]=2)[CH:3]=[N:2]1.[CH3:12][Mg]Br>C1COCC1>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH:10]([OH:11])[CH3:12])[CH:8]=2)[CH:3]=[N:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 185383681H-Indazole-6-carbaldehydeHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 687611451-(1H-Indazol-6-yl)ethanol수율 60.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 1H-indazole-6-carbaldehyde (200 mg, 1.37 mmol) in THF (7 mL) at −78° C. was added methyl magnesium bromide (1.4 mL, 4.11 mmol) dropwise under argon. The solution was warmed to rt and quenched with saturated ammonium chloride (2 mL). The mixture was extracted into ethyl acetate (3×10 mL), dried over MgSO4 and concentrated. The yellow oil was purified by silica gel chromatography (EtOAc/Hex 4:1) to yield the title compound as a clear oil (135 mg, 60%). 1H NMR (400 MHz, CDCl3) δ 8.07 (s, 1H), 7.76 (s, 1H), 7.50-7.47 (m, 2H), 5.05 (q, 1H, J=7.4 Hz), 1.57 (d, 3H, J=7.2 Hz); MS ESI [M+H]+, calcd for [C9H10N2O+H]+ 163.1; found m/z 163.0.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customquenched with saturated ammonium chloride (2 mL)
  2. extractionThe mixture was extracted into ethyl acetate (3×10 mL)
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated
  5. customThe yellow oil was purified by silica gel chromatography (EtOAc/Hex 4:1)

출처 및 근거

ORD 기록
ord-e42229c745e2446bafb7cca923dee6ad
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08765748B2

반응 노트

불러오는 중…