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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846945Generated: October 31, 2026

HCID 58119006, compound → HCID 39080128, compound

https://huagongshe.com/reaction/1846945

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 numberUS08952034B2
Source datasetuspto-grants-2015_02
ORD IDord-222f1fa8b5ca41b9a3a644ce84107f0d
Source noteuspto-grants-2015_02