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Dichloromethane → HCID 178424071, 화합물

HRID 1353753
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HRID 1353753 반응식
Br[C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]3[N:15]=[CH:14][N:13](C(C4C=CC=CC=4)(C4C=CC=CC=4)C4C=CC=CC=4)[N:12]=3)[CH:9]=2)[N:4](C2CCCCO2)[N:3]=1.[CH3:41][C:42]1[CH:47]=[CH:46][C:45](B(O)O)=[CH:44][CH:43]=1.ClCCl.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>COCCOC.C1(P(C2C=CC=CC=2)[C-]2C=CC=C2)C=CC=CC=1.[C-]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=C1.[Fe+2]>[CH3:41][C:42]1[CH:47]=[CH:46][C:45]([C:2]2[C:10]3[C:5](=[CH:6][CH:7]=[C:8]([C:11]4[N:15]=[CH:14][NH:13][N:12]=4)[CH:9]=3)[NH:4][N:3]=2)=[CH:44][CH:43]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 6344DichloromethaneHCID 62657Potassium Phosphate, TribasicHCID 79799Tolylboronic acidHCID 22479811HCID 22479811, 화합물

생성물 1

HCID 178424071HCID 178424071, 화합물수율 185.9%

시약·촉매·용매 2

HCID 635956
Ferrocene-1,1'-bis-(diphenylphosphine)
촉매
HCID 80711,2-Dimethoxyethane용매

실험 절차

To a solution of 2-{3-bromo-5-[1-(triphenylmethyl)(1,2,4-triazol-3-yl)]-1H-indazolyl}perhydro-2H-pyran (0.150 g, 0.254 mmol), in ethylene glycol dimethyl ether (3 mL) was added 4-methylphenyl boronic acid (0.052 g, 0.381 mmol), [1,1′-bis(diphenylphosphino)-ferrocene] complex with dichloromethane (1:1) (0.030 g, 0.0254 mmol) and potassium phosphate (0.269 g, 1.27 mmol). The reaction mixture was heated to reflux temperature for 5 hours. The solvent was then evaporated to dryness and the residue was dissolved in 20 mL of ethyl acetate. The heterogeneous solution was washed 3 times with 10 mL of water and once with 10 mL of brine. The organic layer was dried over Na2SO4 and evaporated to dryness. The resulting brown solid was adsorbed on silica gel and purified by column chromatography (85:15 hexanes/ethyl acetate) to provide the title compound (0.130 g, 85% yield): ES-MS (m/z) 602 [M+1]+.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux temperature for 5 hours
  3. customThe solvent was then evaporated to dryness
  4. dissolutionthe residue was dissolved in 20 mL of ethyl acetate
  5. washThe heterogeneous solution was washed 3 times with 10 mL of water
  6. dry with materialThe organic layer was dried over Na2SO4
  7. customevaporated to dryness
  8. custompurified by column chromatography (85:15 hexanes/ethyl acetate)

출처 및 근거

ORD 기록
ord-efad0ace1294457ea86ed781d138e75e
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07220771B2

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