ChemicalBook > Product Catalog >Organic Chemistry >Heterocyclic Compounds >1-ethyl-1H-pyrazol-4-amine

1-ethyl-1H-pyrazol-4-amine

1-ethyl-1H-pyrazol-4-amine Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Accela ChemBio Co.,Ltd.  
Tel: 021-50795510 4000665055
Email: marketing@accelachem.com
Company Name: QINGDAO CARELONGPHARMATECH CO.,LTD  
Tel: 053288191853 13061484198
Email: sales@carelongchem.com
Company Name: Shanghai Topbiochem Technology Co., Ltd  
Tel: 021-58170097
Email: info@topbiochem.com
Company Name: Shanghai T&W Pharmaceutical Co., Ltd.  
Tel: +86 21 61551611
Email:
1-ethyl-1H-pyrazol-4-amine Basic information
Product Name:1-ethyl-1H-pyrazol-4-amine
Synonyms:1-ethyl-1H-pyrazol-4-amine;1-ethyl-1H-pyrazol-4-amine(SALTDATA: HCl);4-Amino-1-ethylpyrazole;1-ethyl-1H-pyrazol-4-amine hydrochloride;4-Amino-1-ethyl-1H-pyrazole;1H-Pyrazol-4-amine, 1-ethyl-;1-ethylpyrazol-4-amine
CAS:876343-24-7
MF:C5H9N3
MW:111.15
EINECS:
Product Categories:
Mol File:876343-24-7.mol
1-ethyl-1H-pyrazol-4-amine Structure
1-ethyl-1H-pyrazol-4-amine Chemical Properties
Boiling point 238.6±13.0 °C(Predicted)
density 1.16±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka3.72±0.10(Predicted)
AppearancePurple to black Liquid
CAS DataBase Reference876343-24-7
Safety Information
HazardClass IRRITANT
HS Code 2933199090
MSDS Information
1-ethyl-1H-pyrazol-4-amine Usage And Synthesis
Uses1-ethyl-1H-pyrazol-4-amine can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.
SynthesisSynthesis_876343-24-7
General Procedure for the Synthesis of 4-Amino-l-N-alkylated-pyrazolesA solution of 4-nitropyrazole (300mg, 2.65mmol), potassium carbonate (2eq) and the alkylating reagent (l .leq) in acetonitrile (lOmL) was heated at 60C for 18h. After cooling to rt the mixture was diluted with EtOAc and washed with water. The organic phase was collected, dried (MgS04) and concentrated in vacuo. The crude residue was dissolved in methanol (lOmL), palladium on carbon (50mg) was added and the reaction was stirred under a balloon of hydrogen for 18h. The resulting mixture was filtered through Celite and the filtrate concentrated in vacuo to give the desired product. Procedure B:Example 11: 2-((6-( 1 -Ethyl- 1 H-pyrazo 1-4-ylamino)- 1 H-pyrazo lo [3 ,4-d]pyrimidin- 1 -yl) methyl)benzonitrileThe following compound was made according to the procedure in Example 1, using 1-ethyl- lH-pyrazo 1-4-amine. 1 -ethyl- lH-pyrazol-4-amine was prepared by Procedure A using ethyl iodide as alkylating agent: 1H NMR (d6-DMSO) | 9.94 (s, 1H), 8.94 (s, 1H), 8.10 (s, 2H), 7.91 (dd, 1H), 7.66 (td, 1H), 7.49-7.53 (m, 2H), 7.35-7.37 (m, 1H), 5.76 (s, 2H), 4.11 (q, 2H), 1.35 (t, 3H); LC-MS method B, (ES+) 345.1, RT = 8.58min.
1-ethyl-1H-pyrazol-4-amine Preparation Products And Raw materials
Raw materials1H-pyrazole, 1-ethyl-4-nitro--->4-Nitropyrazole-->Iodoethane
Tag:1-ethyl-1H-pyrazol-4-amine(876343-24-7) Related Product Information
4-Phenylpyrazole 1-(4-Chlorophenyl)-3-hydroxy-1H-pyrazole Pyrazole 1-Benzyl-1H-pyrazol-4-amine 1-Benzyl-1H-pyrazol-4-amine hydrochloride 1-Ethyl-1H-pyrazol-4-amine hydrochloride