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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945643Generated: October 29, 2026

Sodium triacetoxyborohydride → HCID 59606149, compound

https://huagongshe.com/reaction/1945643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Methylazetidin-3-olHCID 11542782—
Reactant(2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehydeHCID 59605819—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59606149HCID 5960614945%

Reaction Steps

To a solution of (2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehyde (150 mg, 0.51 mmol) in DCE (10 mL) was added 3-methyl-azetidin-3-ol (65 mg, 0.75 mmol) and powdered 4 Å molecular sieves. The reaction mixture was stirred at room temperature for 2 h, sodium triacetoxyborohydride (215 mg, 1.01 mmol) was added and the resulting mixture stirred for a further 17 h. The reaction mixture was loaded onto an Isolute® SCX-2 cartridge, washed with MeOH then the desired product eluted with 2 M NH3 in MeOH. 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 (83 mg, 45%). LCMS (Method H): RT=2.29 min, [M+H]+ 367.5

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-cd99f2e702ef4683a22601322717a647
Source noteuspto-grants-2013_03