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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657155Generated: October 29, 2026

Sodium triacetoxyborohydride → HCID 68993740, compound

https://huagongshe.com/reaction/657155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(6-methoxy-3-oxopyrido(2,3-b)pyrazin-4(3H)-yl)acetaldehydeHCID 57815220—
ReactantHCID 68991151HCID 68991151—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 68993740HCID 6899374055%

Reaction Steps

To cis-2-{[(3RS,5SR)-5-(methyloxy)-3-piperidinyl]methyl}-1H-isoindole-1,3(2H)-dione (125 mg, 0.43 mmol) in MeOH (1 ml) and CHCl3 (5 ml) was added [6-(methyloxy)-3-oxopyrido[2,3-b]pyrazin-4(3H)-yl]acetaldehyde (for a preparation see Example 126(e)) (100 mg; 0.50 mmol) and the reaction was allowed to stir at room temperature under N2 for 4 hours. Na(OAc)3BH (210 mg; 1.0 mmol) was added and the reaction was allowed to stir at room temperature under nitrogen for an additional 14 hours. The reaction was partitioned between saturated aqueous NaHCO3 (5 mL) and CH2Cl2 (20 mL), the aqueous layer was further extracted with CH2Cl2 (20 mL), and the combined organic layers were dried over Na2SO4. The solvents were removed and the crude residue was purified by chromatography on silica gel using a 0-10% MeOH/DCM gradient to provide the desired compound (10 mg; 55%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-9961a5a0e1524a45af57b55729cd2f92
Source noteuspto-grants-2011_12