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CAS RN: 4023-02-3 | Product Number: A2055
1-Amidinopyrazole Hydrochloride
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Purity: >98.0%(T)(HPLC)
Synonyms:
- Praxadine
- 1-Pyrazolecarboxamidine Hydrochloride
- Pyrazole-1-carboximidamide Hydrochloride
- 1-Carbamimidoylpyrazole Hydrochloride
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days |
|---|---|---|---|
| 5G |
$29.00
|
16 | ≥40 |
| 25G |
$86.00
|
38 | ≥40 |
* Please contact our distributors or
TCI
to order our products. The above prices do not include freight cost, customs, and other charges to the destination.
* The storage conditions are subject to change without notice.
| 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 |
|
| 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:
| H.S.code* | 2933.19-000 |
Application
TCI Practical Example: Guanidinylation of Amine Using Praxadine
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Used Chemicals
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Procedure
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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.
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Experimenter’s Comments
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The reaction mixture was monitored by LC/MS.
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Analytical Data
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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).
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Lead Reference
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- Synthesis and pharmacological characterization of a new benzoxazole derivative as a potent 5-HT3 receptor agonist
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%).
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
- P. L. Lopez-Tudanca, L. Labeaga, A. Innerarity, L. Alonso-Cires, I. Tapia, R. Mosquera, A. Orjales, Bioorg. Med. Chem. 2003, 11, 2709.
- Y. Zhang, A. J. Kennan, Org. Lett. 2001, 3, 2341.
- A. Porcheddu, G. Giacomelli, A. Chighine, S. Masala, Org. Lett. 2004, 6, 4925.
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