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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386142Generated: October 27, 2026

Azidomethyl 2,2-dimethylpropanoate → [4-(4-(Aminocarbonyl)-5-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}-2-thienyl)-1H-1,2,3-triazol-1-yl]methyl pivalate

https://huagongshe.com/reaction/386142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzidomethyl 2,2-dimethylpropanoateHCID 11521126—
ReactantSodium AscorbateHCID 23667548—
Reactant5-Ethynyl-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamideHCID 59526270—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product[4-(4-(Aminocarbonyl)-5-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}-2-thienyl)-1H-1,2,3-triazol-1-yl]methyl pivalateHCID 59525795—

Reaction Steps

5-Ethynyl-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamide (86 mg, 0.25 mmol) and azidomethyl pivalate (59 mg, 0.38 mmol) were combined in DMF (1.0 mL). CuSO4.5H2O (6.3 mg, 0.025 mmol) in water (0.2 mL) and sodium ascorbate (20 mg, 0.10 mmol) in water (0.2 mL) were added, and the reaction mixture was stirred at room temperature overnight. The reaction was concentrated to dryness, combined with MeOH and silica gel, and evaporated. Flash chromatography (dry load, 0-10% MeOH/EtOAc) afforded the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-028dfb019ee4490d9fcb863bbe8ba9f0
Source noteuspto-grants-2013_02