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Water → 1-[4-(3,4-Difluoro-1H-pyrrol-1-yl)-2-fluorophenyl]-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one

HRID 1407328
Notes
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Reaction equation

HRID 1407328 reaction equation
CC([O-])(C)C.[K+].[F:7][C:8]1[CH:13]=[C:12]([N:14]2[CH2:18][C:17](F)([F:19])[C:16](F)([F:21])[CH2:15]2)[CH:11]=[CH:10][C:9]=1[N:23]1[CH:28]=[C:27]([O:29][CH3:30])[C:26](=[O:31])[C:25]([C:32]2[N:36]([C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=3)[N:35]=[CH:34][CH:33]=2)=[N:24]1.O>CS(C)=O>[F:21][C:16]1[C:17]([F:19])=[CH:18][N:14]([C:12]2[CH:11]=[CH:10][C:9]([N:23]3[CH:28]=[C:27]([O:29][CH3:30])[C:26](=[O:31])[C:25]([C:32]4[N:36]([C:37]5[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=5)[N:35]=[CH:34][CH:33]=4)=[N:24]3)=[C:8]([F:7])[CH:13]=2)[CH:15]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 23665647Potassium tert-butoxideHCID 468487401-[2-fluoro-4-(3,3,4,4-tetrafluoropyrrolidin-1-yl)phenyl]-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one

Product 1

HCID 468489141-[4-(3,4-Difluoro-1H-pyrrol-1-yl)-2-fluorophenyl]-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-oneYield 32.4%

Reagents, catalysts & solvents 1

HCID 679
Dimethyl Sulfoxide
Solvent

Procedure

KOtBu (236 mg, 2.1 mmol) was added portionwise at room temperature to a solution of 1-[2-fluoro-4-(3,3,4,4-tetrafluoropyrrolidin-1-yl)phenyl]-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one (352 mg, 0.7 mmol) in DMSO (3.5 mL). After stirring for 30 min, the reaction mixture was poured into water and extracted with AcOEt. The extract was washed with brine, dried over MgSO4, and concentrated under reduced pressure. The residue was subjected to basic silica gel column chromatography eluting with hexane/AcOEt (1/1-0/1) followed by purification by preparative HPLC. Recrystallization from MeOH/H2O afforded the title compound (105 mg, 32% yield) as a white solid: mp 212-214° C.; 1H NMR (300 MHz, CDCl3): δ ppm 3.91 (3H, s), 6.42 (1H, t, J=9.0 Hz), 6.68-6.78 (2H, m), 6.87 (1H, ddd, J=1.1, 2.6, 9.0 Hz), 7.07 (1H, dd, J=2.6, 12.4 Hz), 7.33 (1H, d, J=2.3 Hz), 7.36-7.48 (5H, m), 7.78-7.79 (2H, m). LC-MS (ESI) m/z 464 [M+H]+. Anal. Calcd for C24H16F3N5O2: C, 62.20; H, 3.48; N, 15.11. Found: C, 62.20; H, 3.51; N, 15.01.

Workup

  1. extractionextracted with AcOEt
  2. washThe extract was washed with brine
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated under reduced pressure
  5. washeluting with hexane/AcOEt (1/1-0/1)
  6. customfollowed by purification by preparative HPLC
  7. customRecrystallization from MeOH/H2O

Sources & evidence

ORD record
ord-c6b8d95c97464d48a2c03bba7036b087
Source dataset
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08916566B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes