PIPERIDINE-1-SULFONYL CHLORIDE
PIPERIDINE-1-SULFONYL CHLORIDE Basic information
- Product Name:
- PIPERIDINE-1-SULFONYL CHLORIDE
- Synonyms:
-
- piperidine-1-sulfonyl chloride(SALTDATA: FREE)
- Piperadine-1-sulfonylchloride
- N-piperidinylsulfaMoyl chloride
- 1-Piperidinesulfonylchloride
- Piperidinesulfonyl chloride
- Piperidinosulfonyl chloride
- Piperidine-1-Sulfonic Acid
- Piperidine-1-sulfonyl chloride 96%
- CAS:
- 35856-62-3
- MF:
- C5H10ClNO2S
- MW:
- 183.66
- Mol File:
- 35856-62-3.mol
PIPERIDINE-1-SULFONYL CHLORIDE Chemical Properties
- Boiling point:
- 120℃ (10 Torr)
- Density
- 1.308 g/mL at 25 °C
- refractive index
- 1.4920
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- pka
- -8.25±0.20(Predicted)
- form
- liquid
- color
- Dark brown
- Sensitive
- Moisture Sensitive
- InChIKey
- QQJYAXDCMMXECR-UHFFFAOYSA-N
- CAS DataBase Reference
- 35856-62-3
Safety Information
- Hazard Codes
- C
- Risk Statements
- 34
- Safety Statements
- 26-36/37/39-45
- RIDADR
- UN 3265 8 / PGII
- WGK Germany
- 3
- HazardClass
- 8
- HazardClass
- IRRITANT
- PackingGroup
- Ⅱ
- HS Code
- 2933399990
PIPERIDINE-1-SULFONYL CHLORIDE Usage And Synthesis
Uses
Piperidine-1-sulfonyl chloride is used as pharmaceutical intermediate.
Synthesis
110-89-4
35856-62-3
Example 1: Synthesis of piperidine-1-sulfonyl chloride A mixture of piperidine (100 g, 1.17 mol) and triethylamine (178 g, 1.76 mol) in dichloromethane (500 ml) was slowly added to a solution of sulfuryl chloride (238 g, 1.76 mol) in dichloromethane (500 ml) at 0 °C - 5 °C. The reaction mixture was gradually warmed to room temperature and stirred continuously for 2 hours. After completion of the reaction, the mixture was quenched by pouring into ice water. The organic layer was separated and washed with distilled water (2 x 5 v/v). The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give an oily residue (151.3 g, 70% yield). The resulting product was characterized by nuclear magnetic resonance hydrogen spectroscopy (H NMR): H NMR (300 MHz, CDCl3) δ = 1.58-1.62 (m, 2H), 1.69-1.83 (m, 4H), 3.31-3.42 (m, 4H).
References
[1] Patent: WO2015/83066, 2015, A1. Location in patent: Page/Page column 11-12
[2] Journal of Fluorine Chemistry, 1982, vol. 20, p. 425 - 438
[3] Patent: WO2005/87721, 2005, A2. Location in patent: Page/Page column 81-82
[4] Archiv der Pharmazie (Weinheim, Germany), 1958, vol. 291, p. 7,11
[5] Bulletin de la Societe Chimique de France, 1936, vol. <5> 3, p. 2143,2146, 2149, 2150
PIPERIDINE-1-SULFONYL CHLORIDESupplier
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- 18270980682
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PIPERIDINE-1-SULFONYL CHLORIDE(35856-62-3)Related Product Information
- 3-Hydroxypiperidine hydrochloride
- 1-Aminopiperidine
- 4-PIPERIDINECARBOXYLIC ACID T-BUTYL ESTER HCL
- 4-Piperidinyl(1-pyrrolidinyl)Methanone hydrochloride
- Rosin
- Morpholine
- METHYL PIPECOLINATE HYDROCHLORIDE
- piperidin-4-ylMethanesulfonaMide
- Piperidinium acetate
- METHYL 1-(CHLOROSULFONYL)PIPERIDINE-4-CARBOXYLATE
- PIPERIDINE-1-SULFONYL CHLORIDE
- 3,5-DIMETHYLPIPERIDINE-1-SULFONYL CHLORIDE
- 4-(aminocarbonyl)piperidine-1-sulfonyl chloride
- 2,6-dimethylpiperidine-1-sulfonyl chloride
- ETHYL 1-(CHLOROSULFONYL)PIPERIDINE-2-CARBOXYLATE
- OCTAHYDROISOQUINOLINE-2(1H)-SULFONYL CHLORIDE
- 2-METHYLPIPERIDINE-1-SULFONYL CHLORIDE
- 3-METHYLPIPERIDINE-1-SULFONYL CHLORIDE