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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405064Generated: October 27, 2026

Acetic Acid → HCID 86676406, compound

https://huagongshe.com/reaction/405064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylateHCID 1514400—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86676397HCID 86676397—
Solvent1,2-DichloroethaneHCID 11—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86676406HCID 86676406—

Reaction Steps

To a solution of tert-butyl 4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-formyl-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysen-9-yl)benzoate (0.1 g, 0.167 mmol) in DCE (2 ml) was added acetic acid (0.019 ml, 0.334 mmol) and 4-N-(2-Aminoethyl)-1-N-Boc-piperazine (0.077 g, 0.334 mmol). The mixture was stirred at rt for 2 h then to the mixture was added sodium triacetoxyborohydride (0.177 g, 0.835 mmol). The mixture was stirred for 3 days at rt then was diluted with 7 ml of sat. NaHCO3 and was extracted with dichloromethane (3×7 ml). The combined organic layers were dried with Na2SO4. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure. The crude product was used in the next step without further purification. LCMS: m/e 812.3 (M+H)+, 3.30 min (method 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748415B2
Source datasetuspto-grants-2014_06
ORD IDord-d956ff8daff541d48f27d569066004ab
Source noteuspto-grants-2014_06