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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175180Generated: November 2, 2026

Hydrochloric Acid → HCID 11644329, compound

https://huagongshe.com/reaction/1175180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromineHCID 24408—
ReactantMethyl pyridine-1(2H)-carboxylateHCID 11007981—
ReactantHCID 178454308HCID 178454308—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 11644329HCID 1164432971%

Reaction Steps

A solution of Br2 (0.73 ml, 14.3 mmol, 1 equiv.) in DMF (5 ml) is added over 15 min to a solution of N-methoxycarbonyl-1,2-dihydropyridine 1 (2 g, 14.3 mmol, 1 equiv.) and of Boc-guanidine (9.15 g, 57.5 mmol, 4 equiv.) in a mixture of DMF (10 ml) and of CH3CN (5 ml) under cold conditions (0-5° C.) and under argon. The reaction being complete from the end of the addition of bromine, the reaction mixture is poured onto ice-cold water (600 ml). The aqueous phase is subsequently extracted with DCM (3×200 ml). The crude product obtained (3.5 g) is dissolved in the minimum amount of methanol, followed by addition of a 2N hydrochloric acid solution (10 ml). The solution is brought to reflux in [illegible] for 5 min. After cooling, the reaction mixture is washed with ether and then evaporated to dryness to give 2.4 g of the deprotected compound 4 with a yield of 71% over the two stages.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838681B2
Source datasetuspto-grants-2010_11
ORD IDord-749aceefba14416d8302d2b50060dec8
Source noteuspto-grants-2010_11