1-Butanol → HCID 178428248, compound
Reaction equation
[CH3:1][C:2]1[CH:6]=[C:5]([NH:7][C:8]2[CH:13]=[C:12](Cl)[N:11]=[C:10]([S:15][C:16]3[CH:21]=[CH:20][C:19]([NH:22][C:23]([CH:25]4[CH2:27][CH2:26]4)=[O:24])=[CH:18][C:17]=3[F:28])[N:9]=2)[NH:4][N:3]=1.Cl.C[CH2:31][N:32](C(C)C)[CH:33](C)C.[CH2:39]([OH:43])[CH2:40][CH2:41][CH3:42]>CCOC(C)=O>[CH3:1][C:2]1[CH:6]=[C:5]([NH:7][C:8]2[CH:13]=[C:12]([N:32]3[CH2:33][C:39]([CH:40]4[CH2:42][CH2:41]4)([OH:43])[CH2:31]3)[N:11]=[C:10]([S:15][C:16]3[CH:21]=[CH:20][C:19]([NH:22][C:23]([CH:25]4[CH2:27][CH2:26]4)=[O:24])=[CH:18][C:17]=3[F:28])[N:9]=2)[NH:4][N:3]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 130 °C
Procedure
A mixture of N-(4-(4-(3-methyl-1H-pyrazol-5-ylamino)-6-chloropyrimidin-2-ylthio)-3-fluorophenyl)cyclopropane-carboxamide (160 mg, 0.38 mmol), 3-cycloropylazetidin-3-ol hydrochloride (70 mg, 0.49 mmol) and DIPEA (0.20 ml) in n-butanol (1.5 ml) were heated in microwave at 130 ° C. for 1 h. Reaction mixture was then cooled to room temperature, diluted with EtOAc (20 ml), washed with sat NaHCO3 solution (10 ml), water (2×10 ml), brine (10 ml), dried (MgSO4), filtered and evaporated in vacuo. Crude product was purified by flash chromatography on silica (EtOAc/Petrol 30 to 80%) to give the title compound as a white solid (55 mg, 29%). 1H NMR (DMSO-d6) 0.33-0.36 (2H, m), 0.42-0.48 (2H, m), 0.82-0.86 (4H, m), 1.21-1.24 (2H, m), 1.85-1.89 (1H, m), 2.08 (3H, s), 2.10-2.15 (1H, m), 3.66-3.75 (4H, m), 5.42 (1H, br s), 5.67 (1H, 1H, s), 5.8 (1H, br s), 7.42 (1H, d), 7.52-7.58 (1H, m), 7.75 (1H, d), 9.27 (1H, s), 10.65 (1H, s), 11.9 (1H, br s). ES+ 496.90.
Workup
- customReaction mixture
- temperaturewas then cooled to room temperature
- washwashed
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated in vacuo
- customCrude product was purified by flash chromatography on silica (EtOAc/Petrol 30 to 80%)
Sources & evidence
- ORD record
- ord-02941291fa584144870a6ccc54627bcc
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07528142B2
Reaction notes
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