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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945644Generated: October 26, 2026

Sodium triacetoxyborohydride → 7-[2-(2-Chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)ethyl]-7-azaspiro[3.5]nonan-2-ol

https://huagongshe.com/reaction/1945644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant7-Azaspiro[3.5]nonan-2-olHCID 11171026—
Reactant(2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehydeHCID 59605819—
Solvent1,2-DichloroethaneHCID 11—
Product7-[2-(2-Chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)ethyl]-7-azaspiro[3.5]nonan-2-olHCID 5960536869.5%

Reaction Steps

To a solution of (2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehyde (157 mg, 0.53 mmol) in DCE (10 mL) was added 7-azaspiro[3.5]nonan-2-ol (109 mg, 0.77 mmol) and powdered 4 Å molecular sieves. The reaction mixture was stirred at room temperature for 4 h, sodium triacetoxyborohydride (225 mg, 1.06 mmol) was added and the resulting mixture stirred for a further 16 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% 2 M NH3/MeOH in DCM) to give the title compound as a colourless oil (155 mg, 69%). LCMS (Method H): RT=2.41 min, [M+H]+ 421.5

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-8dfa1614cc2f44fb94203e9075d3260c
Source noteuspto-grants-2013_03