1-Methyl-cyclopropanesulfonic acid amide
1-Methyl-cyclopropanesulfonic acid amide Basic information
- Product Name:
- 1-Methyl-cyclopropanesulfonic acid amide
- Synonyms:
-
- Cyclopropanesulfonamide, 1-methyl- (9CI)
- 1-Methyl-cyclopropanesulfonic acid amide
- 1-MethylCyclopropanesulfonaMide
- 1-Methylcyclopropanesulphonamide
- 1-Methylcyclopropane-1-sulfonamide
- MethylcyclopropylsulfonaMide
- Cyclopropanesulfonamide, 1-methyl-
- 1-METHYL-CYCLOPROPYL SULFONAMIDE
- CAS:
- 669008-26-8
- MF:
- C4H9NO2S
- MW:
- 135.18
- Product Categories:
-
- SULFONAMIDE
- Mol File:
- 669008-26-8.mol
1-Methyl-cyclopropanesulfonic acid amide Chemical Properties
- Melting point:
- 103-104 °C(Solv: hexane (110-54-3))
- Boiling point:
- 246.4±23.0 °C(Predicted)
- Density
- 1.34±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 10.93±0.20(Predicted)
- Appearance
- White to off-white Solid
- InChI
- InChI=1S/C4H9NO2S/c1-4(2-3-4)8(5,6)7/h2-3H2,1H3,(H2,5,6,7)
- InChIKey
- ATJVVVCODTXRAE-UHFFFAOYSA-N
- SMILES
- C1(C)(S(N)(=O)=O)CC1
1-Methyl-cyclopropanesulfonic acid amide Usage And Synthesis
Chemical Properties
Pale yellow liquid
Uses
1-Methyl-cyclopropanesulfonic acid amide is a drug that inhibits the activity of serine protease. It has been shown to inhibit the replication of hepatitis C virus and HIV, while also inhibiting the enzymatic activity of human leukocyte elastase.
Biological Activity
1-Methylcyclopropanesulphonamide binds reversibly to the enzyme's active site with an affinity constant (K) of 7 x 10 M at 37°C and pH 7.5 under conditions where the compound exists in its free form or as a protonated molecule.
Synthesis
849022-29-3
669008-26-8
Step 6: Boc-1-methylcyclopropanesulfonamide 2d6 (151.8 mg, 0.65 mmol) was dissolved in dichloromethane (6 mL) and trifluoroacetic acid (6 mL) was added slowly. The reaction mixture was stirred at room temperature for 3.5 hours. Upon completion of the reaction, the solvent was removed by high vacuum evaporation to afford the deprotected product 2d7 as an off-white waxy solid (79.1 mg, 91% yield). The structure of the product was confirmed by 1H NMR (CDCl3, 400 MHz): δ 4.56 (s, 2H), 1.58 (s, 3H), 1.43-1.38 (m, 2H), 0.85-0.80 (m, 2H).
References
[1] Patent: US9527885, 2016, B2. Location in patent: Page/Page column 617
[2] Patent: US9643999, 2017, B2. Location in patent: Page/Page column 68; 69
[3] Patent: WO2006/7700, 2006, A1. Location in patent: Page/Page column 81
[4] Patent: US2006/19905, 2006, A1. Location in patent: Page/Page column 36
[5] Patent: WO2007/9227, 2007, A1. Location in patent: Page/Page column 43
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