홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

p-Toluenesulfonic acid → 1'-methyl-6'-(1H-pyrazol-4-yl)-1'H-spiro [cyclopentane-1,2'-thieno[3,2-d]pyrimidin]-4'(3'H)-one

HRID 2364024
노트
인쇄 미리보기

반응식

HRID 2364024 반응식
Cl.Cl.[CH3:3][NH:4][C:5]1[CH:9]=[C:8]([C:10]2[CH:11]=[N:12][NH:13][CH:14]=2)[S:7][C:6]=1[C:15]([NH2:17])=[O:16].C([O-])(O)=O.[Na+].[C:23]1(=O)[CH2:27][CH2:26][CH2:25][CH2:24]1.CC1C=CC(S(O)(=O)=O)=CC=1.[O-]S([O-])(=O)=O.[Mg+2]>CN(C=O)C.CCOC(C)=O>[CH3:3][N:4]1[C:5]2[CH:9]=[C:8]([C:10]3[CH:14]=[N:13][NH:12][CH:11]=3)[S:7][C:6]=2[C:15](=[O:16])[NH:17][C:23]21[CH2:27][CH2:26][CH2:25][CH2:24]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 6101p-Toluenesulfonic acidHCID 8452CyclopentanoneHCID 24083Sulfuric acid magnesium salt (1:1)HCID 516892Sodium Bicarbonate2회HCID 667434043-(methylamino)-5-(1H-pyrazol-4-yl)thiophene-2-carboxamide dihydrochloride

생성물 1

HCID 66743852
1'-methyl-6'-(1H-pyrazol-4-yl)-1'H-spiro [cyclopentane-1,2'-thieno[3,2-d]pyrimidin]-4'(3'H)-one
수율 53.3%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 3-(methylamino)-5-(1H-pyrazol-4-yl)thiophene-2-carboxamide dihydrochloride (145 mg, 0.491 mmol), saturated aqueous NaHCO3 (50 mL) and EtOAc (50 mL) was shaken well. The organic layer was collected, dried over MgSO4, filtered and concentrated under reduced pressure. This residue was mixed with cyclopentanone (2.00 mL, 22.6 mmol), PTSA (9.34 mg, 0.049 mmol), MgSO4 (118 mg, 0.982 mmol) and DMF (2 mL). This mixture was stirred at 80° C. overnight. The mixture was poured into saturated aqueous NaHCO3 and extracted with 3:1 EtOAc/THF (100 mL), and the extract was dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (Purif, silica gel, 95:5 hexane/EtOAc to EtOAc then to 90:10 EtOAc/MeOH) to afford a yellow solid. This solid was triturated with EtOAc, and the precipitate was collected by filtration to afford the title compound (75.4 mg, 53%) as a yellow solid:

후처리

  1. customThe organic layer was collected
  2. dry with materialdried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. stirringThis mixture was stirred at 80° C. overnight
  6. extractionextracted with 3:1 EtOAc/THF (100 mL)
  7. dry with materialthe extract was dried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by column chromatography (Purif, silica gel, 95:5 hexane/EtOAc to EtOAc
  11. customto 90:10 EtOAc/MeOH) to afford a yellow solid
  12. customThis solid was triturated with EtOAc
  13. filtrationthe precipitate was collected by filtration

출처 및 근거

ORD 기록
ord-0d656d4d77c5404fa7cdca9e8c8b40d6
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08691828B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트