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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229338Generated: October 29, 2026

Thionyl Chloride → HCID 18466605, compound

https://huagongshe.com/reaction/2229338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Amino-2-chloro-6-picolineHCID 2734415—
Reactant5-Bromo-2-chloro-3-pyridinecarbonyl chlorideHCID 12677295—
ReactantHCID 178418525HCID 178418525—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 18466605HCID 1846660531%

Reaction Steps

NaHCO3 (3.9 g, 46.4 mmol) was added to a solution of 3-amino-2-chloro-6- methylpyridine (2.2 g, 15.4 mmol; prepared as described by K. G. Grozinger et al. J. Heterocyclic Chem. 1995,32,259-263) in MeCN (50 mL). The resulting suspension was stirred for 15 min. and a solution of crude 5-bromo-2-chloro-3-pyridinecarbonyl chloride (prepared from 5-bromo-2-hydroxy-3-pyridinecarboxylic acid and SOCl2 [as described by T. W. Gero et al. in Synth. Commun. 1989, 19, 553-559 (incorporated herein by reference) but with omission of the aqueous work-up] (4 g,) in MeCN (10 mL) was introduced over 30 min. The resulting suspension was stirred at room temperature. After 24 h, the mixture was poured into a mixture of water (100 mL) and ice (10 g) and stirred for 20 min. The suspension was filtered and the resulting solid was washed with water (50 mL) and hexane (25 mL), then dried over P2O5 under reduced pressure to give the title compound (1.8 g, 31% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420359B1
Source datasetuspto-grants-2002_07
ORD IDord-64ffff2fae2446a8ab771d7dbb27aa46
Source noteuspto-grants-2002_07