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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217327Generated: October 30, 2026

Ethyl orthoformate → 3-(5-Methyl-pyridin-2-yl)-5-tetrazol-1-yl-benzoic acid methyl ester

https://huagongshe.com/reaction/217327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantSodium AzideHCID 33557—
ReactantMethyl 3-amino-5-(5-methylpyridin-2-yl)benzoateHCID 57851018—
SolventAcetic AcidHCID 176—
Product3-(5-Methyl-pyridin-2-yl)-5-tetrazol-1-yl-benzoic acid methyl esterHCID 57850994100%

Reaction Steps

To a solution of 3-amino-5-(5-methyl-pyridin-2-yl)-benzoic acid methyl ester (362 mg, 1.51 mmol) and NaN3 (182 g, 2.8 mmol) in AcOH was added HC(OEt)3 (1074 mg, 7.25 mmol) at room temperature. The reaction mixture was heated to reflux for 4 hours and then cooled to room temperature. The solvent was removed in vacuo and the residue was purified by silica-gel chromatography to give 3-(5-methyl-pyridin-2-yl)-5-tetrazol-1-yl-benzoic acid methyl ester as a light yellow solid (440 mg, 100%). MS (M+H)=296.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193368B2
Source datasetuspto-grants-2012_06
ORD IDord-f5766d6344194a3f87c769b6bf0481d0
Source noteuspto-grants-2012_06