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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205739Generated: October 29, 2026

HCID 58119006, compound → HCID 39080128, compound

https://huagongshe.com/reaction/2205739

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 numberUS09371329B2
Source datasetuspto-grants-2016_06
ORD IDord-f6561c2602d5452da18bc2052d02f0b3
Source noteuspto-grants-2016_06