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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Methoxide → 3-Pyridinamine, 4-chloro-2-methoxy-

HRID 1260456
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HRID 1260456 반응식
Br[C:2]1[C:7]([NH2:8])=[C:6]([Cl:9])[CH:5]=[CH:4][N:3]=1.[CH3:10][O-:11].[Na+]>CO>[Cl:9][C:6]1[CH:5]=[CH:4][N:3]=[C:2]([O:11][CH3:10])[C:7]=1[NH2:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10942334Sodium Methoxide2회HCID 224762862-Bromo-4-chloropyridin-3-amine

생성물 1

HCID 451221783-Pyridinamine, 4-chloro-2-methoxy-

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a stirred solution of 2-bromo-4-chloropyridin-3-amine (prepared as described in US2002/0119982) (1.0 eq.) in dry MeOH (0.25M) under argon was added a solution of NaOMe (25% wt in MeOH, 1.5 eq.) and the reaction mixture was refluxed for 1 h, more NaOMe (25% wt in MeOH, 1.5 eq) was added and the reaction mixture was refluxed for an additional 2 h. The volatiles were removed under reduced pressure and the crude product was purified by flash chromatography eluting with 2-10% EtOAc/petroleum ether affording the titled compound as yellow oil. 1H-NMR (300 MHz, DMSO-d6, 300K) δ 7.33 (1H, d, J=5.5 Hz), 6.88 (1H, d, J=5.5 Hz), 5.13 (2H, bs), 3.89 (3H, s). MS (ES) C6H7ClN2O requires: 158, found: 159, 161 (M+H)+.

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후처리

  1. temperaturethe reaction mixture was refluxed for 1 h
  2. temperaturethe reaction mixture was refluxed for an additional 2 h
  3. customThe volatiles were removed under reduced pressure
  4. customthe crude product was purified by flash chromatography
  5. washeluting with 2-10% EtOAc/petroleum ether affording the titled compound as yellow oil

출처 및 근거

ORD 기록
ord-4752c620a0ce476781a4744e822ba63a
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08470823B2

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