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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182057Generated: November 4, 2026

5-Aminothiophene-2-sulfonamide → 4-[5-Bromo-4-(1-hydroxymethyl-propylamino)-pyrimidin-2-ylamino]-thiophene-2-sulfonic acid amide

https://huagongshe.com/reaction/1182057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminothiophene-2-sulfonamideHCID 24711598—
Reactant4-Aminothiophene-2-sulfonamideHCID 45080588—
Reactant(R)-2-(2-chloro-5-bromopyrimidine-4-ylamino)butan-1-olHCID 58891316—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product4-[5-Bromo-4-(1-hydroxymethyl-propylamino)-pyrimidin-2-ylamino]-thiophene-2-sulfonic acid amideHCID 69332142—

Reaction Steps

530 mg (1.9 mmol) of (R)-2-(5-bromo-2-chloro-pyrimidin-4-ylamino)-butan-1-ol is added to a suspension of 303 mg of a mixture that consists of 4-amino-thiophene-2-sulfonic acid amide and 5-amino-thiophene-2-sulfonic acid amide (ratio: 2:1) in 7 ml of ethanol and 170 μl of concentrated HCl. The reaction mixture is stirred for 21 hours under reflux. After cooling, the batch is purified by chromatography (Flashmaster II, hexane/EE 2:8). The crude product that is obtained is then recrystallized (ethyl acetate/diisopropyl ether). 47 mg (0.11 mmol, 7% of theory) of the product 4-[5-bromo-4-(1-hydroxymethyl-propylamino)-pyrimidin-2-ylamino]-thiophene-2-sulfonic acid amide is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288547B2
Source datasetuspto-grants-2007_10
ORD IDord-2da2ba2ba2ef4b8289ee8b1b82d63104
Source noteuspto-grants-2007_10