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CAS RN: 4023-02-3 | Product Number: A2055

1-Amidinopyrazole Hydrochloride


Purity: >98.0%(T)(HPLC)
Synonyms:
  • Praxadine
  • 1-Pyrazolecarboxamidine Hydrochloride
  • Pyrazole-1-carboximidamide Hydrochloride
  • 1-Carbamimidoylpyrazole Hydrochloride
Product Documents:
5G
¥3,100
16   13   ≥40 
25G
¥9,400
38   ≥40  Contact Us
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Product Number A2055
Purity / Analysis Method >98.0%(T)(HPLC)
Molecular Formula / Molecular Weight C__4H__6N__4·HCl = 146.58 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN 4023-02-3
Reaxys Registry Number 5448758
PubChem Substance ID 87559963
MDL Number

MFCD00210087

Specifications
Appearance White to Yellow to Orange powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(Nonaqueous Titration) min. 98.0 %
Melting point 165.0 to 169.0 °C
Properties (reference)
Melting Point 167 °C
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P302 + P352 : IF ON SKIN: Wash with plenty of water.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
Related Laws:
Transport Information:
Application
TCI Practical Example: Guanidinylation of Amine Using Praxadine

TCI Practical Example: Guanidinylation of Amine Using Praxadine

Used Chemicals

Procedure

A solution of 4-bromophenethylamine (200 mg, 1.00 mmol), DIEA (509 µL, 3.00 mmol) and praxadine (147 mg, 1.00 mmol) in DMF (1.7 mL) was stirred at ambient temperature for 2 days. The reaction mixture was concentrated and the residue was washed with dichloromethane/2-propanol (4:1 (vol/vol)). The guanidinylated compound 1 was obtained as a pale yellow solid (164 mg, 67% yield.) after filtration.

Experimenter’s Comments

The reaction mixture was monitored by LC/MS.

Analytical Data

Guanidinylated Compound 1

1H NMR (270 MHz, DMSO-d6); δ 7.57 (t, J = 6.3 Hz, 1H), 7.52 (d, J = 8.4 Hz, 2H), 7.25 (d, J = 8.4 Hz, 2H), 6.99 (brs, 3H), 3.35 (q, J = 6.3 Hz, 2H), 2.76 (t, J = 6.3 Hz, 2H).

Lead Reference


Application
Guanidinylation

Typical Procedure:
1-Amidinopyrazole hydrochloride (1 g, 6.8 mmol) is added to a solution of 2-(benzoxazol-2-yl)ethylamine (1.1 g, 6.7 mmol) and diisopropylethylamine (4.75 mL, 27 mmol) in DMF (10 mL). The reaction mixture is stirred at room temperature under N2 for 24 h. Subsequently, diethylether (75 mL) is added, the upper layer is decanted and the remaining oil solidified by treatment with CH2Cl2. The solid is collected, washed with diethylether, CH2Cl2, and CHCl3 : i-PrOH (4 : 1) and dried to yield the product (0.86 g, Y. 52.6%).

References


PubMed Literature


Product Documents (Note: Some products will not have analytical charts available.)
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