Potassium Carbonate → 3-(5-Ethynyl-1,3,4-oxadiazol-2-yl)-5-(4-isopropylsulfonylphenyl)pyrazin-2-amine

HRID 78663

반응식

HRID 78663 반응식
BrP(Br)(C1C=CC=CC=1)(C1C=CC=CC=1)[C:3]1[CH:8]=CC=C[CH:4]=1.C[Si](C)(C)C#CC(O)=O.[NH2:31][C:32]1[C:33]([C:50]([NH:52][NH2:53])=[O:51])=[N:34][C:35]([C:38]2[CH:43]=[CH:42][C:41]([S:44]([CH:47]([CH3:49])[CH3:48])(=[O:46])=[O:45])=[CH:40][CH:39]=2)=[CH:36][N:37]=1.CCN(C(C)C)C(C)C.C(=O)([O-])[O-].[K+].[K+]>C(#N)C.C(OCC)(=O)C.O>[C:3]([C:8]1[O:51][C:50]([C:33]2[C:32]([NH2:31])=[N:37][CH:36]=[C:35]([C:38]3[CH:39]=[CH:40][C:41]([S:44]([CH:47]([CH3:49])[CH3:48])(=[O:45])=[O:46])=[CH:42][CH:43]=3)[N:34]=2)=[N:52][N:53]=1)#[CH:4]

참가 물질

9

반응물 5

HCID 11430Potassium CarbonateHCID 70579Triphenylphosphine dibromideHCID 81531DiisopropylethylamineHCID 27608633-(Trimethylsilyl)propiolic AcidHCID 594716323-Amino-6-(4-isopropylsulfonylphenyl)pyrazine-2-carbohydrazide

생성물 1

HCID 594719483-(5-Ethynyl-1,3,4-oxadiazol-2-yl)-5-(4-isopropylsulfonylphenyl)pyrazin-2-amine수율 27%

시약·촉매·용매 3

HCID 962Water용매HCID 6342Acetonitrile용매HCID 8857Ethyl Acetate용매

실험 절차

Dibromo(triphenyl)phosphorane (1.208 g, 2.862 mmol) was added to a suspension of 3-trimethylsilylprop-2-ynoic acid (84.8 mg, 0.60 mmol) and 3-amino-6-(4-(isopropylsulfonyl)phenyl)pyrazine-2-carbohydrazide (200 mg, 0.60 mmol) in acetonitrile (3.000 mL) at room temperature and the resulting solution stirred for 30 min. DIPEA (385.4 mg, 519.4 μL, 2.982 mmol) was then added and a precipitate quickly formed. The resulting mixture was stirred at room temperature for 1 h and was then filtered. The reaction mixture was concentrated in vacuo and the residue taken up in methanol (5 mL) and potassium carbonate (131.9 mg, 0.9541 mmol) added and the resulting solution stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate (5 mL) and water (5 mL) and the layers separated. The aqueous layer was extracted further with ethyl acetate (2×5 mL), dried over MgSO4 and concentrated in vacuo. The material was purified by reverse phase preparative HPLC [Waters Sunfire C18, 10 μM, 100 Å column, gradient 10%-95% B (solvent A: 0.05% TFA in water; solvent B: CH3 CN) over 16 minutes at 25 mL/min]. Product fractions were freeze dried to leave the product as a yellow solid (56.1 mg, 27% yield); 1H NMR (400 MHz, DMSO) d 1.18 (m, 6H), 3.44 (m, 1H), 5.48 (s, 1H), 7.96 (m, 2H), 8.32 (m, 2H) and 9.08 (s, 1H) ppm; MS (ES+) 370.14

후처리

  1. customa precipitate quickly formed
  2. stirringThe resulting mixture was stirred at room temperature for 1 h
  3. filtrationwas then filtered
  4. concentrationThe reaction mixture was concentrated in vacuo
  5. stirringthe resulting solution stirred at room temperature overnight
  6. customthe layers separated
  7. extractionThe aqueous layer was extracted further with ethyl acetate (2×5 mL)
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated in vacuo
  10. customThe material was purified by reverse phase preparative HPLC [Waters Sunfire C18, 10 μM, 100 Å column, gradient 10%-95% B (solvent A: 0.05% TFA in water; solvent B: CH3 CN) over 16 minutes at 25 mL/min]
  11. customdried

출처 및 근거

ORD 기록
ord-2c19f68ab2f64991bf4e7943b952fa91
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08841308B2

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