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

Sodium Methoxide → 7-[(Methylsulfanyl)methyl]-1H-indole

HRID 561372
노트
인쇄 미리보기

반응식

HRID 561372 반응식
C(OC([N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][C:15]=2[CH2:17][S:18][CH3:19])[CH:10]=[CH:9]1)=O)(C)(C)C.C[O-].[Na+]>CO>[CH3:19][S:18][CH2:17][C:15]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:16]=1[NH:8][CH:9]=[CH:10]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 58392224HCID 58392224, 화합물

생성물 1

HCID 583921877-[(Methylsulfanyl)methyl]-1H-indole

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1.16 g (4.18 mmol) of the compound from Example 7A were introduced into 23 ml of methanol, 26 ml (113 mmol) of a 25% strength methanolic sodium methanolate solution were added, and the mixture was stirred at RT overnight. Then ice-water was added, and the mixture was extracted with dichloromethane. The organic phase was dried over magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography (mobile phase: cyclohexane/ethyl acetate gradient) to result in 549 mg (74% of theory) of the title compound.

후처리

  1. additionwere added
  2. extractionthe mixture was extracted with dichloromethane
  3. dry with materialThe organic phase was dried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was purified by flash chromatography (mobile phase: cyclohexane/ethyl acetate gradient)

출처 및 근거

ORD 기록
ord-b9c1050cb38e45e789e8595762e561af
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063234B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트