4-Hydrazinobenzoic acid methyl ester hydrochloride

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4-Hydrazinobenzoic acid methyl ester hydrochloride Basic information
Product Name:4-Hydrazinobenzoic acid methyl ester hydrochloride
Synonyms:AURORA 1803;Benzoic acid, 4-hydrazino-, Methyl ester, Monohydrochloride;Methyl 4-hydrazinylbenzoate hydrochloride;methyl 4-hydrazinobenzoate hydrochloride;Benzoic acid,4-hydrazinyl-, methyl ester, hydrochloride (1:1);Dilarozil (Methylhydrazine Hydrochloride);4-Hydrazinobenzoic acid methyl ester hydrochloride
CAS:6296-89-5
MF:C8H11ClN2O2
MW:202.64
EINECS:
Product Categories:
Mol File:6296-89-5.mol
4-Hydrazinobenzoic acid methyl ester hydrochloride Structure
4-Hydrazinobenzoic acid methyl ester hydrochloride Chemical Properties
Melting point 205-207 °C
storage temp. Inert atmosphere,Room Temperature
AppearanceOff-white to light brown Solid
InChIInChI=1S/C8H10N2O2.ClH/c1-12-8(11)6-2-4-7(10-9)5-3-6;/h2-5,10H,9H2,1H3;1H
InChIKeyMXSGRGCOQOKOEH-UHFFFAOYSA-N
SMILESC1(C(=O)OC)C=CC(NN)=CC=1.Cl
Safety Information
MSDS Information
4-Hydrazinobenzoic acid methyl ester hydrochloride Usage And Synthesis
UsesMethyl 4-hydrazinylbenzoate HCl
Synthesis
2-hydrazinobenzoic acid

5326-27-2

4-HYDRAZINOBENZOIC ACID METHYL ESTER HYDROCHLORIDE

6296-89-5

General procedure for the synthesis of methyl 4-hydrazinylbenzoate hydrochloride from 2-hydrazinylbenzoic acid: 4M dioxane solution of hydrogen chloride (100 mL, 399.60 mmol) was slowly added to a solution of 2-hydrazinylbenzoic acid (15.2 g, 99.90 mmol) in methanol (200 mL). The reaction mixture was stirred at 90 °C for 5 hours. Upon completion of the reaction, it was cooled to 20 °C and the resulting precipitate was collected by filtration, washed with ether (100 mL) and subsequently dried under vacuum to afford the target product methyl 4-hydrazinobenzoate hydrochloride (16.50 g, 82% yield) as a milky white crystalline solid. Mass spectrometry analysis (ESI-) showed m/z (M-H)- = 165; high performance liquid chromatography (HPLC) retention time was 1.12 min. 1H NMR (400.13 MHz, DMSO-d6) δ 3.81 (3H, s, OCH3), 6.99-7.02 (2H, m, Ar-H), 7.86-7.90 (2H, m, Ar- H), 8.98 (1H, s, NH), 10.47 (3H, s, NH3+).

References[1] Patent: WO2008/99145, 2008, A1. Location in patent: Page/Page column 155-156
[2] Patent: WO2008/99145, 2008, A1. Location in patent: Page/Page column 156
4-Hydrazinobenzoic acid methyl ester hydrochloride Preparation Products And Raw materials
Raw materials2-hydrazinobenzoic acid-->Methanol-->1,4-Dioxane-->Hydrochloric acid
Preparation Products2-Methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole-8-carboxylic acid methyl ester
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