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Tetrahydrofuran → HCID 71272190, 화합물

HRID 475151
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HRID 475151 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:12]#[N:13])[C:5]2[C:6](I)=[N:7][NH:8][C:9]=2[CH:10]=1.[O:14]1[CH:19]=[CH:18][CH2:17][CH2:16][CH2:15]1.[CH2:20]1COCC1>>[Cl:1][C:2]1[CH:3]=[C:4]([C:12]#[N:13])[C:5]2[C:6]([CH3:20])=[N:7][N:8]([CH:19]3[CH2:18][CH2:17][CH2:16][CH2:15][O:14]3)[C:9]=2[CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 8028TetrahydrofuranHCID 80803,4-dihydro-2H-pyranHCID 178509895HCID 178509895, 화합물

생성물 1

HCID 71272190HCID 71272190, 화합물수율 78.4%

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온도
80 °C

실험 절차

A mixture of 6-chloro-3-iodo-1H-indazole-4-carbonitrile (2.0 g, 6.59 mmol), dihydropyran (1.09 g, 13.18 mmol), and TsOH monohydrate (127 mg, 0.659 mmol) in THF (40 mL) under nitrogen was heated at 80° C. overnight. The reaction mixture was quenched with water (40 mL) and extracted with EtOAc (50 mL×3). The combined extracts were washed with brine, dried (MgSO4), filtered, and concentrated in vacuo. The residue was purified by SiO2 chromatography eluting with petroleum ether/EtOAc (5:1) to afford 6-chloro-3-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-4-carbonitrile as white solid (2 g, 78.4%). MS (ESI): m/z=388 [M+1]+.

후처리

  1. customThe reaction mixture was quenched with water (40 mL)
  2. extractionextracted with EtOAc (50 mL×3)
  3. washThe combined extracts were washed with brine
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by SiO2 chromatography
  8. washeluting with petroleum ether/EtOAc (5:1)

출처 및 근거

ORD 기록
ord-ed7f39dc97e4480692fc6f8dd4f74e4e
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637537B2

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