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Sodium bis(trimethylsilyl)amide → 6-Chloro-4-[(R)-1-(5-fluoro-2-methoxy-phenyl)-ethoxy]-pyridazin-3-ylamine

HRID 1406276
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HRID 1406276 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:11][CH3:12])=[C:6]([C@H:8]([OH:10])[CH3:9])[CH:7]=1.N[N:14]1[CH:19]=[C:18](Br)[CH:17]=[C:16]([Cl:21])[NH:15]1.C[Si](C)(C)[N-:24][Si](C)(C)C.[Na+]>O1CCCC1>[Cl:21][C:16]1[N:15]=[N:14][C:19]([NH2:24])=[C:18]([O:10][C@@H:8]([C:6]2[CH:7]=[C:2]([F:1])[CH:3]=[CH:4][C:5]=2[O:11][CH3:12])[CH3:9])[CH:17]=1
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참가 물질

5

반응물 3

HCID 2724254Sodium bis(trimethylsilyl)amideHCID 26597266(1R)-1-(5-fluoro-2-methoxyphenyl)ethan-1-olHCID 674671712-Amino-4-bromo-6-chloro-pyridazine

생성물 1

HCID 866910956-Chloro-4-[(R)-1-(5-fluoro-2-methoxy-phenyl)-ethoxy]-pyridazin-3-ylamine수율 54%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
66 °C

실험 절차

To a solution of (R)-1-(5-fluoro-2-methoxy-phenyl)-ethanol (4.78 g, 28 mmol, 1.5 eq.) in tetrahydrofuran (40 mL) was added 2-amino-4-bromo-6-chloro-pyridazine (3.9 g, 18.7 mmol) followed by a solution of sodium hexamethyldisilazide (1M in tetrahydrofuran, 28.1 mL, 1.5 eq.). This mixture was then heated to 66° C. for 18 hr before cooling and evaporating under reduced pressure. The residue was purified by chromatography on silica gel (150 g) eluting with a gradient of ethyl acetate in heptane (10:90 to 50:50) to give the title compound as a yellow solid (3.0 g, 54%).

후처리

  1. temperaturebefore cooling
  2. customevaporating under reduced pressure
  3. customThe residue was purified by chromatography on silica gel (150 g)
  4. washeluting with a gradient of ethyl acetate in heptane (10:90 to 50:50)

출처 및 근거

ORD 기록
ord-167e7b9864614f0084cde8f97e331ce5
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916593B2

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