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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874429Generated: October 27, 2026

Hydrochloric Acid → Methyl 2-amino-5H,6H,7H,8H-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylate

https://huagongshe.com/reaction/874429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantMethyl 2-amino-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylateHCID 68474008—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-amino-5H,6H,7H,8H-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylateHCID 90383449107.7%

Reaction Steps

Platinum(IV) oxide (3 g) was added to a mixed solution of methanol (200 ml), methylene chloride (200 ml), and concentrated hydrochloric acid (3.9 ml) containing the methyl 2-amino-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylate (3.0 g) obtained in (Example 5.16) <Step 1>. The obtained mixture was stirred in a hydrogen atmosphere for 66 hours at room temperature. Thereafter, the reaction solution was filtered with Celite, and was then washed with methanol (80 ml). The filtrate was combined with the washing solution, and the thus mixed solution was then concentrated under reduced pressure. The obtained residue was subjected to azeotropy with methanol (20 ml) four times, so as to obtain the title compound (3.3 g) in the form of a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980889B2
Source datasetuspto-grants-2015_03
ORD IDord-1f73abe8d1454d389cd9154b2b37a776
Source noteuspto-grants-2015_03