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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182053Generated: October 25, 2026

Hydrochloric Acid → 5-[5-Bromo-4-(cyclopropylmethyl-amino)-pyrimidin-2-ylamino]-pyridine-2-sulfonic acid amide

https://huagongshe.com/reaction/1182053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant5-Aminopyridine-2-sulfonamideHCID 22313850—
Reactant(5-Bromo-2-chloro-pyrimidin-4-yl)-cyclopropylmethyl-amineHCID 58891001—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
Product5-[5-Bromo-4-(cyclopropylmethyl-amino)-pyrimidin-2-ylamino]-pyridine-2-sulfonic acid amideHCID 10453519—

Reaction Steps

263 mg (1.0 mmol) of (5-bromo-2-chloro-pyrimidin-4-yl)-cyclopropylmethyl-amine is dissolved in 2 ml of acetonitrile and added to a suspension of 172 mg (1.0 mmol) of 5-amino-pyridine-2-sulfonic acid amide (representation according to W. T. Caldwell, E. C. Kornfeld J. Am. Chem. Soc. 1942, 64, 1695-1698) in 1 ml of acetonitrile, 0.25 ml of a 4 molar solution of hydrochloric acid in 1,4-dioxane as well as 0.25 ml of water. The reaction mixture is stirred under reflux overnight. After cooling, the precipitate that is formed is filtered off and washed with warm water. After drying, 286 mg (0.72 mmol, 72% of theory) of the product 5-[5-bromo-4-(cyclopropylmethyl-amino)-pyrimidin-2-ylamino]-pyridine-2-sulfonic acid amide is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288547B2
Source datasetuspto-grants-2007_10
ORD IDord-bc58274207c24976b77aa43814b048b4
Source noteuspto-grants-2007_10