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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203393Generated: October 31, 2026

1-Bromo-3-methanesulfonylpropane → (3-{5-Cyano-2-[(R)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-2,3,5,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-5-yl]-phenyl}-propyl)-(3-methanesulfonyl-propyl)-dimethyl-ammonium formate

https://huagongshe.com/reaction/2203393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-methanesulfonylpropaneHCID 51892082—
Reactant(R)-5-[4-Cyano-2-(3-dimethylamino-propyl)-phenyl]-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-2,3,5,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidine-6-carboxylic acid methyl esterHCID 76284943—
SolventAcetonitrileHCID 6342—
Product(3-{5-Cyano-2-[(R)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-2,3,5,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-5-yl]-phenyl}-propyl)-(3-methanesulfonyl-propyl)-dimethyl-ammonium formateHCID 7628498965.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of Example 12 (150 mg, 0.28 mmol) in MeCN (2 mL) was added 1-bromo-3-methanesulfonyl-propane (225 mg, 1.12 mmol). The resulting mixture was heated at 90° C. for 40 minutes using microwave irradiation. The solvent was removed in vacuo and the resultant residue was purified by reverse phase chromatography (MDAP), giving the title compound as an off-white solid (65 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365577B2
Source datasetuspto-grants-2016_06
ORD IDord-e463bc89a36e4ad39ac774f7e77172df
Source noteuspto-grants-2016_06