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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621169Generated: October 30, 2026

2-Aminopyridine → 56000-35-2

https://huagongshe.com/reaction/1621169

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
SolventDichloromethaneHCID 6344—
Product56000-35-2HCID 1226419082.4%

Reaction Steps

To a suspension of O-(mesitylsulfonyl)hydroxylamine (9.2 g, 42.7 mmol) in dichloromethane (110 mL) was added pyridin-2-amine (4.02 g, 42.7 mmol) in four portions at 0-5° C. to give a yellow solution. After 5 min the yellow solution turned into a light yellow suspension. The ice bath was removed after 10 min and the reaction mixture was stirred at RT for 1 h. The suspension was diluted with diethyl ether (100 mL), filtered, washed with diethyl ether and dried in vacuo to give the product (10.9 g, 35.2 mmol, 82.4%) as light red solid which was used without further purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772510B2
Source datasetuspto-grants-2014_07
ORD IDord-43e33c7c78274cb99f3f8b054f19d093
Source noteuspto-grants-2014_07