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

Pyridine → N-{3-[5-(2-amino-4-pyrimidinyl)-2-(1,1-dimethylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2-pyridinesulfonamide

HRID 590308
Notes
Print preview

Reaction equation

HRID 590308 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[S:7]([O-:9])=[O:8].[Na+].ClN1C(=O)CCC1=O.S(Cl)(Cl)(=O)=O.[NH2:24][C:25]1[C:26]([F:47])=[C:27]([C:31]2[N:32]=[C:33]([C:43]([CH3:46])([CH3:45])[CH3:44])[S:34][C:35]=2[C:36]2[CH:41]=[CH:40][N:39]=[C:38]([NH2:42])[N:37]=2)[CH:28]=[CH:29][CH:30]=1.N1C=CC=CC=1>ClCCl>[NH2:42][C:38]1[N:37]=[C:36]([C:35]2[S:34][C:33]([C:43]([CH3:45])([CH3:46])[CH3:44])=[N:32][C:31]=2[C:27]2[C:26]([F:47])=[C:25]([NH:24][S:7]([C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=3)(=[O:9])=[O:8])[CH:30]=[CH:29][CH:28]=2)[CH:41]=[CH:40][N:39]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 1049PyridineHCID 24648Sulfuryl chlorideHCID 31398ChlorosuccinimideHCID 23678794Sodium Pyridine-2-sulfinateHCID 579897094-[4-(3-Amino-2-fluorophenyl)-2-(1,1-dimethylethyl)-1,3-thiazol-5-yl]-2-pyrimidinamine

Product 1

HCID 57989786
N-{3-[5-(2-amino-4-pyrimidinyl)-2-(1,1-dimethylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2-pyridinesulfonamide
Yield 12.4%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a suspension of sodium 2-pyridinesulfinate (48.4 mg, 0.291 mmol) in dichloromethane (3 ml) was added N-chlorosuccinimide (38.9 mg, 0.291 mmol). After 1 hour, the reaction mixture was filtered through a short Celite plug. To the crude sulfonyl chloride solution was added the 4-[4-(3-amino-2-fluorophenyl)-2-(1,1-dimethylethyl)-1,3-thiazol-5-yl]-2-pyrimidinamine (50 mg, 0.146 mmol) and pyridine (0.035 ml, 0.437 mmol), and the mixture was stirred for 3 hours at ambient temperature. After 3 hours, the reaction was quenched with methanol, and the crude reaction mixture was concentrated, redissolved in methanol, and purified via reversed-phase HPLC chromatography, eluting with 30-60% acetonitrile/0.1% aqueous trifluoroacetic acid. The desired fractions were combined, neutralized with aqueous saturated sodium bicarbonate, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated to obtain the title compound (8.8 mg, 12%) as tan solid. MS (ESI): 485 [M+H]+.

Workup

  1. filtrationthe reaction mixture was filtered through a short Celite plug
  2. waitAfter 3 hours
  3. customthe reaction was quenched with methanol
  4. customthe crude reaction mixture
  5. concentrationwas concentrated
  6. dissolutionredissolved in methanol
  7. custompurified via reversed-phase HPLC chromatography
  8. washeluting with 30-60% acetonitrile/0.1% aqueous trifluoroacetic acid
  9. extractionextracted with ethyl acetate
  10. washThe organic layer was washed with brine
  11. dry with materialdried over anhydrous sodium sulfate
  12. filtrationfiltered
  13. concentrationconcentrated

Sources & evidence

ORD record
ord-ab4b5462380b42828fd61f7a1d63159c
Source dataset
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09233956B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes