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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502123Generated: October 30, 2026

Ethyl orthoformate → methyl 2-(4-methyl-5-(1H-tetrazol-1-yl)pyridin-2-yl)acetate

https://huagongshe.com/reaction/1502123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantSodium AzideHCID 33557—
ReactantMethyl 2-(5-amino-4-methyl-2-pyridinyl)acetateHCID 89619043—
SolventAcetic AcidHCID 176—
SolventSodium chloride; waterHCID 57417360—
Productmethyl 2-(4-methyl-5-(1H-tetrazol-1-yl)pyridin-2-yl)acetateHCID 89619214—

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl 2-(5-amino-4-methylpyridin-2-yl)acetate (90 mg, 0.499 mmol) was stirred in acetic acid (3 ml) then added triethyl orthoformate (0.166 ml, 0.999 mmol) and sodium azide (58.4 mg, 0.899 mmol). The mixture was stirred at 80° C. for 3 hrs then diluted with brine and extracted with ethyl acetate. The organic layer was dried over Na2SO4, filtered and evaporated to dryness. The residue was chromatographed thru 40 g ISCO Redi-sep column and eluted with 5% MeOH/DCM to yield methyl 2-(4-methyl-5-(1H-tetrazol-1-yl)pyridin-2-yl)acetate: 1H-NMR (500 MHz, CDCl3) δ ppm 8.867 (s, 1H), 8.527 (s, 1H), 7.438 (s, 1H), 3.963 (s, 2H), 3.790 (s, 3H), 2.308 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-68345b8e318f4292a36cba76f16918c7
Source noteuspto-grants-2015_12