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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350645Generated: October 25, 2026

Sodium Hydroxide → 3-{4-[6-(Cyclopropylmethyl-amino)-pyridin-3-yl]-1,2,3-triazol-1-yl}-4-methyl-benzoic acid

https://huagongshe.com/reaction/1350645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-Azido-4-methylbenzoic acidHCID 17973091—
Reactant2-(Cyclopropylmethyl)amino-5-ethynyl pyridineHCID 21097278—
ReactantSodium AscorbateHCID 23667548—
CatalystCopper SulfateHCID 24462—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-{4-[6-(Cyclopropylmethyl-amino)-pyridin-3-yl]-1,2,3-triazol-1-yl}-4-methyl-benzoic acidHCID 2109729466.7%

Reaction Steps

3-Azido-4-methyl benzoic acid (497 mg; 2.81 mmol) was suspended in 6.5 mL of EtOH. To this mixture was added 4N NaOH until the mixture became homogeneous, followed then by 2-(cyclopropylmethyl)amino-5-ethynyl pyridine (460 mg; 2.61 mmol) and 529 mg (2.67 mmol) of sodium ascorbate in 0.7 mL of water. The mixture was stirred rapidly as 2.67 mL of a 0.1 M CuSO4 solution was added. A yellow precipitate formed and the mixture was stirred rapidly for 14 h. The mixture was poured into water and acidified carefullly with HOAc. The resulting precipitate was filtered and washed with water. A fine yellow powder was isolated. This material was crushed in 1 mL of MeOH and 5 mL of NH4OH was added. The resulting green mixture was stirred for 10 min, then HOAc was carefully added until a white precipitate formed (pH 8–9). The precipitate was filtered and washed with 1% HOAc in water, then with water and hexanes to provide 607 mg (1.74 mmol; 65%) of 3-{4-[6-(cyclopropylmethyl-amino)-pyridin-3-yl]-1,2,3-triazol-1-yl}-4-methyl-benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214802B2
Source datasetuspto-grants-2007_05
ORD IDord-402bf39638c849a58fd0ec86ba6eac5a
Source noteuspto-grants-2007_05