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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357331Generated: October 29, 2026

Triethylamine → 2-Hydrazino-5-(methanesulfonyl)-pyridine

https://huagongshe.com/reaction/1357331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-Bromo-5-(methylsulfonyl)pyridineHCID 9899483—
SolventWaterHCID 962—
Product2-Hydrazino-5-(methanesulfonyl)-pyridineHCID 996429386%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of 2-bromo-5-(methanesulfonyl)-pyridine (27.5 g, 116 mmol), triethylamine (14.7 g. 145 mmol), and hydrazine hydrate (7.26 g, 145 mmol) in water (205 ml) was heated to 70° C. The reaction mixture became homogenous before the product started to precipitate out of this mixture (after 90 minutes). The reaction mixture was stirred at 70° C. for total of 5 hours and then was allowed to cool to room temperature and stirred for 18 hours. The precipitated product was collected by filtration, dried and triturated with hot ethanol to afford 2-hydrazino-5-(methanesulfonyl)-pyridine in 86% yield. 1H NMR (300 MHz, CDCI3) δ3.12 (s, 3H), 4.44 (br s, 2H), 6.80 (br d, J=8.7 Hz. 1H), 7.81 (dd. J1=9.0 Hz, J2=2.4 Hz, 1H), 8.38 (d, 2.3 Hz, 1H), 8.57 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06590103B2
Source datasetuspto-grants-2003_07
ORD IDord-c8f8f1c43e524cbcbc622e65c5c1257c
Source noteuspto-grants-2003_07