2-Naphthylhydrazine hydrochloride Chemical Properties

Melting point:

123°C

storage temp. 

under inert gas (nitrogen or Argon) at 2-8°C

solubility 

DMSO (Slightly), Water (Slightly)

form 

Solid

color 

White to Off-White

InChI

InChI=1S/C10H10N2.ClH/c11-12-10-7-3-5-8-4-1-2-6-9(8)10;/h1-7,12H,11H2;1H

InChIKey

FYSSYOCJFZSKNW-UHFFFAOYSA-N

SMILES

NNC1=C2C(C=CC=C2)=CC=C1.[H]Cl

CAS DataBase Reference

2243-58-5(CAS DataBase Reference)

Safety Information

HS Code 

2928009090

2-Naphthylhydrazine hydrochloride Usage And Synthesis

Chemical Properties

Pale yellow powder

Uses

2-Naphthylhydrazine Hydrochloride acts as a reagent in the synthesis and biological activity of some new pyrazoline and pyrimidine derivatives as antibacterial and antifungal agents. Synthesis and biological evaluation of 6-hydroxypyridazinone derivatives as σ1 receptor ligands for treating neuropathic pain.

Synthesis

2.1 Synthesis of 2-naphthylhydrazine hydrochloride To a suspension of 2-naphthylamine (800 mg, 5.59 mmol) in hydrochloric acid (6.0 M, 6 mL), a solution of sodium nitrite (NaNO2, 578 mg, 8.38 mmol) in water (1.2 mL) was slowly added under cooling conditions in a water-ice bath (addition time was 2 min). The reaction mixture was stirred in a water-ice bath for 1 h, followed by the slow addition of stannous chloride (SnCl2, 3.71 g, 19.56 mmol) (addition time was 5 min). The resulting suspension was continued to be stirred in a water-ice bath for 3.5 h, followed by filtration. The filter cake was washed sequentially with ice water (0°C, 4 × 8 mL), room temperature water (1 × 8 mL), ice ether (0°C, 2 × 4 mL), and ether/hexane (1:1, 2 × 4 mL) and hexane (2 × 5 mL). The solid was dried to give 690 mg of the target product (Rf = 0.7, 40% ethyl acetate/hexane unfolding agent, milky white solid, 63% yield). 1H NMR (DMSO-d6, 250 MHz, δ): 7.81 (m, 2H, ArH), 7.71 (d, J = 7.7 Hz, 1H, ArH), 7.49-7.19 (m, 4H, ArH). MS-El+ m/z: 159.1 (M-HCl+1).

References

[1] Patent: EP2395003, 2011, A1. Location in patent: Page/Page column 12; 17-18
[2] Journal of Medicinal Chemistry, 1990, vol. 33, # 6, p. 1714 - 1720
[3] Angewandte Chemie - International Edition, 2014, vol. 53, # 20, p. 5202 - 5205
[4] Angew. Chem., 2014, vol. 126, # 20, p. 5303 - 5306,4

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