Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749677Generated: October 30, 2026

Acetic Acid → HCID 178451827, compound

https://huagongshe.com/reaction/1749677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-butyl 4-[[(Z)-[amino-[5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl]methylidene]amino]carbamoyl]piperidine-1-carboxylateHCID 90283740—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178451827HCID 17845182770%

Reaction Conditions

Temperature70 °C

Reaction Steps

Acetic acid (200 mL) was added to dioxane (500 mL) in a 3 L fixed double jacketed vessel and the solution was heated to 70° C. under nitrogen. (Z)-tert-butyl 4-(2-(amino(5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl)methylene)hydrazinecarbonyl)-piperidine-1-carboxylate (74.5 g, 152.80 mmol) was added portionwise to the warm mixture. After 10 minutes the temperature was increased to 100° C. (slight reflux). The reaction mixture was stirred at 100° C. for 1.5 hours (suspension) then held at 80° C. overnight (solution formed after overnight hold). The resulting solution was concentrated under reduced pressure, then diluted with toluene, evaporated to dryness, taken up with toluene and concentrated again. The residual oil was mixed with some ethyl acetate and concentrated to dryness. A solid crystallised from solution which was triturated with MTBE (200 mL) and isolated by filtration. The filter cake was washed with water and MTBE to afford tert-butyl 4-(5-(5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl)-1H-1,2,4-triazol-3-yl)piperidine-1-carboxylate (50 g, 70%) as a grey solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156831B2
Source datasetuspto-grants-2015_10
ORD IDord-c47f8dcf0e6e4dc1a82c7b1fdf1b78fe
Source noteuspto-grants-2015_10