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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406246Generated: October 31, 2026

Acetic Acid → HCID 86667199, compound

https://huagongshe.com/reaction/2406246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4'-Chlorobiphenyl-2-carbaldehydeHCID 1393689—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67980776HCID 67980776—
SolventMethanolHCID 887—
ProductHCID 86667199HCID 8666719964.2%

Reaction Steps

To a vial containing N-(7-azepan-4-yl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazin-3-yl)-4-((R)-3-morpholin-4-yl-1-phenylsulfanylmethyl-propylamino)-3-trifluoromethanesulfonyl-benzenesulfonamide (62 mg, 0.080 mmol) and 4′-chloro-biphenyl-2-carbaldehyde (52.1 mg, 0.241 mmol) was added methanol (2.5 mL) under nitrogen. The reaction was stirred in an ice bath for 10 minutes and then acetic acid (5.51 μL, 0.096 mmol) was added. After stirring in the ice bath for an additional 15 minutes, sodium cyanoborohydride (40.3 mg, 0.642 mmol) was added. The reaction was then allowed to warm to ambient temperature and stir for 72 hours. The reaction mixture was concentrated, filtered and purified via flash chromatography on silica gel (10-50% methanol in CH2Cl2) to afford the title compound (50 mg, 64% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809352B2
Source datasetuspto-grants-2014_08
ORD IDord-c06f963ff41547b587d8c6c4b4a324ff
Source noteuspto-grants-2014_08