HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

2,2-Dimethoxypropane → Cdc7-IN-15

HRID 2364072
Notes
Print preview

Reaction equation

HRID 2364072 reaction equation
[NH2:1][C:2]1[CH:6]=[C:5](Br)[S:4][C:3]=1[C:8]([NH2:10])=[O:9].CO[C:13](OC)([CH3:15])[CH3:14].CC1(C)C2(CS(O)(=O)=O)C(CC1CC2)=O.[O-]S([O-])(=O)=O.[Mg+2].[CH3:39][C:40]1[C:44](B2OC(C)(C)C(C)(C)O2)=[CH:43][N:42](C(OC(C)(C)C)=O)[N:41]=1.C(=O)([O-])[O-].[Na+].[Na+]>O.COCCOC.CC(N(C)C)=O>[CH3:14][C:13]1([CH3:15])[NH:1][C:2]2[CH:6]=[C:5]([C:44]3[CH:43]=[N:42][NH:41][C:40]=3[CH3:39])[S:4][C:3]=2[C:8](=[O:9])[NH:10]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

10

Reactant 6

HCID 64952,2-DimethoxypropaneHCID 10340Sodium CarbonateHCID 18462Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 24083Sulfuric acid magnesium salt (1:1)HCID 219758623-Amino-5-bromothiophene-2-carboxamideHCID 53216815
Tert-butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)-1H-pyrazole-1-carboxylate

Product 1

HCID 66743505Cdc7-IN-15Yield 86%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 80711,2-DimethoxyethaneSolventHCID 31374DimethylacetamideSolvent

Conditions

Temperature
90 °C

Procedure

A mixture of 3-amino-5-bromothiophene-2-carboxamide (1.99 g, 9.0 mmol), 2,2-dimethoxypropane (10 mL), CSA (209 mg, 0.90 mmol), MgSO4 (2.17 g, 18 mmol) and DMA (10 mL) was stirred at 90° C. for 2 h. After removal of MgSO4 by filtration, saturated aqueous NaHCO3 was added to the filtrate. The organic materials were extracted with EtOAc. The combined extracts were washed with water and brine, dried over Na2SO4 and filtered. After removal of the solvent at reduced pressure, a brown crystalline solid was obtained. A flask was charged with this solid, tert-butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate (6.0 g, 19.5 mmol), sodium carbonate (2.3 g, 38.3 mmol), 1,2-dimethoxyethane (30 mL) and water (15 mL). The flask was purged with argon. Then, 1,1′-bis(diphenylphosphino)ferrocenepalladium (II) dichloride dichloromethane adduct (626 mg, 0.766 mmol) was added to the mixture. The flask was purged with argon again. After stirring at 100° C. for 3.5 h, 8 M aqueous NaOH (2.0 mL) was added. After stirring at 100° C. for 1 h, the organic materials were extracted with EtOAc/THF. The combined extracts were dried over Na2SO4 and filtered. After removal of the solvent at reduced pressure, the residue was purified by column chromatography (Purif, silica gel, EtOAc to 90:10 EtOAc/MeOH) to give the title compound (1.97 g, 86%) as a brown solid:

Workup

  1. customAfter removal of MgSO4
  2. filtrationby filtration, saturated aqueous NaHCO3
  3. additionwas added to the filtrate
  4. extractionThe organic materials were extracted with EtOAc
  5. washThe combined extracts were washed with water and brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. customAfter removal of the solvent at reduced pressure
  9. customa brown crystalline solid was obtained
  10. customThe flask was purged with argon
  11. customThe flask was purged with argon again
  12. stirringAfter stirring at 100° C. for 3.5 h
  13. addition8 M aqueous NaOH (2.0 mL) was added
  14. stirringAfter stirring at 100° C. for 1 h
  15. extractionthe organic materials were extracted with EtOAc/THF
  16. dry with materialThe combined extracts were dried over Na2SO4
  17. filtrationfiltered
  18. customAfter removal of the solvent at reduced pressure
  19. customthe residue was purified by column chromatography (Purif, silica gel, EtOAc to 90:10 EtOAc/MeOH)

Sources & evidence

ORD record
ord-1b0d14fe1cef4c11a847ffbd1c845032
Source dataset
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08691828B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes