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Methyl iodide → HCID 61360573, 화합물

HRID 518061
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HRID 518061 반응식
[Cl:1][C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH:10]2[CH2:12][CH2:11]2)[CH:5]=[N:4][CH:3]=1.[CH2:13]([Li])CCC.IC.S([O-])([O-])(=O)=S.[Na+].[Na+]>O1CCCC1>[Cl:1][C:2]1[N:7]=[C:6]([N:8]([CH2:9][CH:10]2[CH2:11][CH2:12]2)[CH3:13])[CH:5]=[N:4][CH:3]=1
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참가 물질

6

반응물 4

HCID 6328Methyl iodideHCID 24477Sodium ThiosulfateHCID 61699309HCID 61699309, 화합물HCID 178418339Butyllithium

생성물 1

HCID 61360573HCID 61360573, 화합물수율 70%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

To a solution of 6-chloro-N-(cyclopropylmethyl)pyrazin-2-amine (0.60 g) in tetrahydrofuran (5 mL) was added dropwise n-butyllithium (3.06 mL, 1.6 M hexane solution) at −78° C. The mixture was stirred at −78° C. for 5 min, and iodomethane (1.02 mL) was added dropwise thereto. The mixture was stirred at −78° C. for 30 min, and further stirred at 0° C. for 1 hr. Saturated aqueous sodium thiosulfate solution (10 mL) was added, and the mixture was extracted with ethyl acetate. The aqueous layer was extracted again with ethyl acetate. The combined organic layer was washed with water and saturated brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography (solvent gradient: 5-*15% ethyl acetate/hexane) to give the title compound (0.46 g, 70%) as a pale-yellow oil.

후처리

  1. stirringThe mixture was stirred at −78° C. for 30 min
  2. stirringfurther stirred at 0° C. for 1 hr
  3. extractionthe mixture was extracted with ethyl acetate
  4. extractionThe aqueous layer was extracted again with ethyl acetate
  5. washThe combined organic layer was washed with water and saturated brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated
  8. customThe residue was purified by silica gel column chromatography (solvent gradient: 5-*15% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-5b347886bd454004b47eaace57d7e4bc
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115139B2

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