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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406433Generated: October 29, 2026

HCID 58119006, compound → HCID 39080128, compound

https://huagongshe.com/reaction/406433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58119006HCID 58119006—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 39080128HCID 39080128—

Reaction Steps

Compound B was prepared by heating A, 6-bromo-3-isopropyl-8-nitro-[1,2,4]triazolo[4,3-a]pyridine, prepared as described in Example 9A, Step 1, (0.777 mmole) in acetic acid (6 mL) in the presence of Zinc dust (3.89 mmole) at 60 C for 1 hour. The reaction mixture was then diluted with methanol and filtered to celite. The filtrate was concentrated down and the residue was then filtered through silica gel with first ethyl acetate and then with 1:4 mixture of methanol and dichloromethane. The filtrate was evaporated in vacuo to yield B, 6-bromo-3-isopropyl-[1,2,4]triazolo[4,3-a]pyridin-8-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754103B2
Source datasetuspto-grants-2014_06
ORD IDord-d687fd6820544f06ac0d61e2aa58819e
Source noteuspto-grants-2014_06