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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696775Generated: November 1, 2026

Sodium hydride → Methyl-6-[({[5-(2-hydroxyethyl)-4-methyl-2-thienyl]sulfonyl}carbamoyl)amino]-4-(trifluoromethyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/1696775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl 6-[({[5-(2-acetoxyethyl)-4-methyl-2-thienyl]sulfonyl}carbamoyl)amino]-4-(trifluoromethyl)pyridine-2-carboxylateHCID 42630611—
SolventMethanolHCID 887—
ProductMethyl-6-[({[5-(2-hydroxyethyl)-4-methyl-2-thienyl]sulfonyl}carbamoyl)amino]-4-(trifluoromethyl)pyridine-2-carboxylateHCID 42630724—

Reaction Steps

To a suspension of 0.100 g methyl 6-[({[5-(2-acetoxyethyl)-4-methyl-2-thienyl]sulfonyl}carbamoyl)amino]-4-(trifluoromethyl)pyridine-2-carboxylate in 1.5 ml methanol was added 0.02 g sodium hydride 55% in oil. The resulting solution was stirred at room temperature for 18 h. The reaction mixture was partitioned between 10% citric acid and ethyl acetate. The phases were separated and the organic phase was washed with brine and evaporated to yield the title compound as white foam. MS (ISN) M−H+=466.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163778B2
Source datasetuspto-grants-2012_04
ORD IDord-8bb789dff0844980a69dbe1faf3b3271
Source noteuspto-grants-2012_04