Pyridine → 2-Chloro-N-[(4-ethyl-4,5-dihydro-pyrazol-1-yl)-methyl-sulfanyl-methylene]benzenesulfon-amide
Reaction equation
[CH2:1]([CH:3]1[CH2:7][NH:6][N:5]=[CH:4]1)[CH3:2].C[S:9][C:10](SC)=[N:11][S:12]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[Cl:21])(=[O:14])=[O:13].N1C=CC=C[CH:25]=1>>[Cl:21][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[S:12]([N:11]=[C:10]([CH3:25])[S:9][N:5]1[CH2:4][CH:3]([CH2:1][CH3:2])[CH:7]=[N:6]1)(=[O:14])=[O:13]Participants
Procedure
500 mg 4-Ethyl-4,5-dihydro-1H-pyrazole was dissolved in 10 mL pyridine. 1.51 g N-(Bis-methylsulfanyl-methylene)-2-chloro-benzenesulfonamide was added and the mixture was refluxed overnight. The mixture was concentrated in vacuo and H2O was added, followed by extraction twice with DCM. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The crude product was purified with flash chromatography (gradient DCM:acetone=100:0 to 95:5) to yield 1.30 g of a yellow oil. 1H NMR (400 MHz, CDCl3) δ 1.02 (t, J=7.5 Hz, 3H), 1.55-1.77 (m, 2H), 2.28 (s, 3H), 3.27-3.39 (m, 1H), 4.13 (dd, J=11.5 and 6.5 Hz, 1H), 4.58 (t, J=11.5 Hz, 1H), 7.16 (d, J=2 Hz, 1H), 7.39 (dt, J=7.5 and 2 Hz, 1H), 7.46 (dt, J=7.5 and 2 Hz, 1H), 7.52 (dd, J=7.5 and 2 Hz, 1H), 8.17 (dd, J=7.5 and 2 Hz, 1H).
Workup
- temperaturethe mixture was refluxed overnight
- concentrationThe mixture was concentrated in vacuo and H2O
- additionwas added
- extractionfollowed by extraction twice with DCM
- dry with materialThe combined organic layers were dried over Na2SO4
- concentrationconcentrated in vacuo
- customThe crude product was purified with flash chromatography (gradient DCM:acetone=100:0 to 95:5)
Sources & evidence
- ORD record
- ord-e6f8b38247c34282b73c14f8fb70fdee
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07728018B2
Reaction notes
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