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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945645Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 59605926, compound

https://huagongshe.com/reaction/1945645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(1-Methylethyl)-3-azetidinolHCID 22163791—
Reactant(2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehydeHCID 59605819—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59605926HCID 5960592633%

Reaction Steps

To a solution of (2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehyde (69 mg, 0.23 mmol) in DCE (5 mL) was added 3-isopropyl-azetidin-3-ol (27 mg, 0.23 mmol) and powdered 4 Å molecular sieves. The reaction mixture was stirred at room temperature for 2 h, sodium triacetoxyborohydride (99 mg, 0.47 mmol) was added and the resulting mixture stirred for a further 2 days. 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% 2 M NH3/MeOH in DCM) to give the title compound as a pale yellow oil (30 mg, 33%). LCMS (Method H): RT=2.65 min, [M+H]+ 395.5

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-4bdd94fb28c846ef96953dfa85b1fd02
Source noteuspto-grants-2013_03