Identification | Back Directory | [Name]
CIS-N-BENZYL-3-METHYLAMINO-4-METHYL-PIPERIDINE BIS-(HYDROCHLORIDE) | [CAS]
1062580-52-2 | [Synonyms]
TOF30 Tofacitinib-1 Tofatinib Impurity 5 Tofacitinib interMediate A Tofacitinib intermediate 3 piperidin-3-amine dihydrochL Tofacitinib Impurity 123 DiHCl Azilsartan medoxomil impurity351 Tofacitinib Impurity 5 Dihydrochloride (3R,4R)-N,4-DiMethyl-1-(phenylMethyl)-3-piperidi (3R,4R)-1-BENZYL-N,4-DIMETHYLPIPERIDIN-3-AMINE 2HCL (3R,4R)-N,4-Dimethyl-1-(benzyl)-3-piperidinamine 2HCl (3R,4R)- Cis-1-benzyl-4-Methyl-3-(MethylaMino)piperidine cis-1-Benzyl-N,4-dimethylpiperidin-3-amine dihydrochloride (3R,4R)-N,4-Dimethyl-1-(phenylmethyl)-3-piperidinamine HCl cis-1-Benzyl-N3,4-dimethylpiperidin-3-amine dihydrochloride Cis-n-benzyl-3-methylamino-4-methyl-piperidine bis-(, HCl ) Cis 1-benzyl-4-methyl-3-methylamino-piperidine hydrochloride (3R,4R)-1-BENZYL-N,4-DIMETHYLPIPERIDIN-3-AMINEDITYDROCHLORIDE (3R,4R)-1-BENZYL-N,4-DIMETHYLPIPERIDIN-3-AMINE DIHYDROCHLORID (3R,4R)-1-BENZYL-N,4-DIMETHYLPIPERIDIN-3-AMINE DIHYDROCHLORIDE (3R,4R)-1-Benzyl-N,4-dimethyl-3-piperidinamine dihydrochloride (3R,4R)-N,4-Dimethyl-1-(phenylmethyl)-3-piperidinamine hydro... (3R,4R)-N,4-Dimethy1-(phenylmethyl)-3-piperidinamine hydrochloride (3R,4R)-1-benzyl-N,4-diMethylpiperidin-3-aMine BIS-(HYDROCHLORIDE) CIS-N-BENZYL-3-METHYLAMINO-4-METHYL-PIPERIDINE BIS-(HYDROCHLORIDE) (3R,4R)-1-Benzyl-3-(methylamino)-4-methylpiperidine Dihydrochloride (3R,4R)-N,4-Dimethyl-1-(phenylmethyl)-3-piperidinamine hydrochloride cis-1-Benzyl-4-methyl-3-(methylamino)piperidine dihydrochloride 95+% (3R,4R)-N, 4-dimethyl-1 -(phenylmethyl) -3-piperidamine hydrochloride (3R,4R)-(1-Benzyl-4-methyl-piperidin-3-yl)-methyl-amine dihydrochloride N-((3R,4R)-N,4-Dimethyl-1-(phenylmethyl)-3-piperidinamine hydrochloride (3R,4R)- cis-1-Benzyl-4-Methyl-3-(MethylaMino)piperidine dihydrochloride 3-Piperidinamine, N,4-dimethyl-1-(phenylmethyl)-, dihydrochloride, (3R,4R)- (3R,4R)-N,4-Dimethyl-1-(phenylmethyl)-3-piperidinamine, hydrochloride (1:2) (3R,?4R)?-N,?4-?Dimethyl-?1-?(phenylmethyl)?-3-?piperidinamine Dihydrochloride 3-PiperidinaMine, N,4-diMethyl-1-(phenylMethyl)-, hydrochloride (1:2), (3R,4R)- CIS-N-BENZYL-3-METHYLAMINO-4-METHYL-PIPERIDINE BIS-(HYDROCHLORIDE) Tofacitinib (Int.) | [Molecular Formula]
C14H24Cl2N2 | [MDL Number]
MFCD11044501 | [MOL File]
1062580-52-2.mol | [Molecular Weight]
291.26 |
Chemical Properties | Back Directory | [Melting point ]
249~251℃ | [storage temp. ]
Inert atmosphere,2-8°C | [solubility ]
Aqueous Acid (Slightly), DMSO (Slightly, Heated, Sonicated), Methanol (Slightly) | [form ]
Solid | [color ]
White to Off-White | [InChI]
InChI=1/C14H22N2.ClH/c1-12-8-9-16(11-14(12)15-2)10-13-6-4-3-5-7-13;/h3-7,12,14-15H,8-11H2,1-2H3;1H/t12-,14+;/s3 | [InChIKey]
FVRZQLQXDPJADE-WLZBWWFYNA-N | [SMILES]
C(C1C=CC=CC=1)N1CC[C@@H](C)[C@@H](NC)C1.Cl |&1:10,12,r| |
Hazard Information | Back Directory | [Uses]
(3R,?4R)?-N,?4-?Dimethyl-?1-?(phenylmethyl)?-3-?piperidinamine Hydrochloride is a related compound of Tofacitinib (T528000). (3R,?4R)?-N,?4-?Dimethyl-?1-?(phenylmethyl)?-3-?piperidinamine Hydrochloride can be used to prepare janus kinase 1 selective inhibitor. | [Uses]
(3R,4R)-1-benzyl-N,4-dimethylpiperidin-3-amine dihydrochloride can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes. | [Synthesis]
![Synthesis_1062580-52-2](/NewsImg/2021-12-27/6377621733007887364937435.jpg) The TiCl4(0.2g, 1mmol), NEt3(0.15g, 1 . 5mmol) suspended 200 ml in toluene, then add 1-benzyl-4-methyl-3-ketone piperidine (20.3g, 100mmol), temperature control 35 ??C methylamine solution is added to the reaction solution (9.32g, 120mmol) reaction 4 hours, adding NaBH (OAC) 3 (0.32g, 1 . 5mmol), glacial acetic acid 2 ml, temperature control 35 ??C reaction, thin layer monitoring after the reaction is complete. Adding saturated salt water washing, anhydrous sodium sulfate for drying the organic phase, the organic phase concentrated, with residues 35% hydrochloric acid ethanol re-crystallization, to obtain (3R, 4R)-cis-1-benzyl-4-methyl-3-methylamino-piperidine dihydrochloride 17.2g, yield 85.0%, optical purity 99.0% (HPLC method). |
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