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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253708Generated: October 26, 2026

Acetic Acid → tert-Butyl 9-(5,6-dihydro-[1,2,4]triazolo[1,5-a]pyrazin-7(8H)-yl)-3-azaspiro[5.5]undecane-3-carboxylate

https://huagongshe.com/reaction/1253708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodiumHCID 5360545—
Reactant5H,6H,7H,8H-(1,2,4)triazolo(1,5-a)pyrazineHCID 18406919—
Reactanttert-Butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylateHCID 51072194—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Producttert-Butyl 9-(5,6-dihydro-[1,2,4]triazolo[1,5-a]pyrazin-7(8H)-yl)-3-azaspiro[5.5]undecane-3-carboxylateHCID 6670111762%

Reaction Steps

Acetic acid (2.34 eq.) was added to a solution of tert-butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylate (1.122 mmol, 1 eq.) and 5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyrazine (1.14 eq.) in methylene chloride (7 ml). Sodium triacetoxyborhydride (1.4 eq) was then added and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with methylene chloride and sat. NaHCO3 solution. The aqueous phase was washed with methylene chloride (2×20 ml), and the combined organic phases were dried over Na2SO4 and concentrated in vacuo. The crude product was purified by column chromatography (silica, ethyl acetate/ethanol 10:1) to obtain the desired product. Yield: 62%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455475B2
Source datasetuspto-grants-2013_06
ORD IDord-14a9f0001dd04364973ca7fee12507fb
Source noteuspto-grants-2013_06