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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945648Generated: November 1, 2026

Sodium triacetoxyborohydride → HCID 59605276, compound

https://huagongshe.com/reaction/1945648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant6-(Propan-2-YL)piperazin-2-oneHCID 10197747—
Reactant(2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehydeHCID 59605819—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59605276HCID 5960527635.6%

Reaction Steps

To a solution of (2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehyde (184 mg, 0.62 mmol) in DCE (15 mL) was added 6-isopropylpiperazin-2-one (106 mg, 0.75 mmol) and powdered 4 Å molecular sieves. The reaction mixture was stirred at room temperature for 6 h, sodium triacetoxyborohydride (364 mg, 1.72 mmol) was added and the resulting mixture stirred for a further 18 h. The reaction mixture was filtered through Celite®, loaded onto an Isolute® SCX-2 cartridge, washed with MeOH then the desired product eluted with 2 M NH3/MeOH in DCM. The resulting residue was purified by column chromatography (Si—PCC, 0-10% MeOH in DCM) to give the title compound as a pale yellow oil (93 mg, 35%). LCMS (Method H): RT=3.44 min, [M+H]+ 422.4

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-38c4614fadf442e7b1f7852cd73a45b5
Source noteuspto-grants-2013_03