Tin dichloride dihydrate → Tert-butyl 3-((5-amino-2-(5-cyanopyrazin-2-ylamino)pyridin-4-ylamino)methyl)piperidine-1-carboxylate

HRID 384656노트

반응식

HRID 384656 반응식
[C:1]([C:3]1[N:4]=[CH:5][C:6]([NH:9][C:10]2[CH:15]=[C:14]([NH:16][CH2:17][CH:18]3[CH2:23][CH2:22][CH2:21][N:20]([C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])[CH2:19]3)[C:13]([N+:31]([O-])=O)=[CH:12][N:11]=2)=[N:7][CH:8]=1)#[N:2].O.[Sn](Cl)Cl>C(O)C>[NH2:31][C:13]1[C:14]([NH:16][CH2:17][CH:18]2[CH2:23][CH2:22][CH2:21][N:20]([C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])[CH2:19]2)=[CH:15][C:10]([NH:9][C:6]2[CH:5]=[N:4][C:3]([C:1]#[N:2])=[CH:8][N:7]=2)=[N:11][CH:12]=1

참가 물질

4

반응물 2

HCID 43835034Tin dichloride dihydrateHCID 66745665Tert-butyl 3-((2-(5-cyanopyrazin-2-ylamino)-5-nitropyridin-4-ylamino)methyl)piperidine-1-carboxylate

생성물 1

HCID 66745373Tert-butyl 3-((5-amino-2-(5-cyanopyrazin-2-ylamino)pyridin-4-ylamino)methyl)piperidine-1-carboxylate수율 56.2%

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
70 °C

실험 절차

tert-Butyl 3-((2-(5-cyanopyrazin-2-ylamino)-5-nitropyridin-4-ylamino)methyl)piperidine-1-carboxylate (265 mg, 0.583 mmol) was dissolved in ethanol (20 mL) and tin (II) chloride hydrate (658 mg, 2.92 mmol) was added. The suspension was heated for 30 min at 70° C. Solvents were removed by evaporation and the residue was dissolved in ethyl acetate and aqueous saturated sodium hydrogen carbonate. The mixture was filtered and the residue was washed thoroughly with ethyl acetate. The two phases of the filtrate were separated and the aqueous phase was extracted twice with ethyl acetate. The combined organic phases were dried (Na2SO4) and solvent was removed by evaporation affording tert-butyl 3-((5-amino-2-(5-cyanopyrazin-2-ylamino)pyridin-4-ylamino)methyl)piperidine-1-carboxylate (139 mg, 56%). The crude product was used directly in the next step.

후처리

  1. customSolvents were removed by evaporation
  2. dissolutionthe residue was dissolved in ethyl acetate
  3. filtrationThe mixture was filtered
  4. washthe residue was washed thoroughly with ethyl acetate
  5. customThe two phases of the filtrate were separated
  6. extractionthe aqueous phase was extracted twice with ethyl acetate
  7. dry with materialThe combined organic phases were dried (Na2SO4) and solvent
  8. customwas removed by evaporation

출처 및 근거

ORD 기록
ord-127fc08f21e3472e9fcd6408ac2c5b4e
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08367658B2

반응 노트

불러오는 중…