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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539251Generated: October 27, 2026

Triethylamine → Azd-8848

https://huagongshe.com/reaction/539251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 2-(3-formylphenyl)acetateHCID 11819590—
ReactantSodiumacetoxyborohydrideHCID 23670382—
Reactant6-Amino-2-butoxy-9-{3-[(3-morpholin-4-ylpropyl)amino]propyl}-7,9-dihydro-8H-purine-8-one dimaleateHCID 86651362—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductAzd-8848HCID 1159222890.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a suspension of 6-amino-2-butoxy-9-{3-[(3-morpholin-4-ylpropyl)amino]propyl}-8-oxo-7,9-dihydro-8H-purine dimaleate (15.00 g, 23.45 mmol) in NMP (54.08 g) was added triethyamine (7.12 g, 70.35 mmol) at 25° C. Then sodium acetoxyborohydride (8.45 g, 39.87 mmol) was added thereto, followed by stirring at 25° C. for 15 minutes. After adding methyl (3-formylphenyl)acetate (6.27 g, 35.18 mol) and stirring at 25° C. for 8 hours, the mixture was cooled to 5° C. and then diluted with cold water (240.00). After adjusting pH to 7 with 10% sodium carbonate solution, a seed crystal was added thereto. After stirring for additional 15 minutes, the mixture was adjusted to pH 8 with 10% sodium carbonate solution and thereto was added water (15 g). After keeping at 5° C. for 1 hour, the resulting white solid was filtered, washed and dried to give the subject compound (12.10 g, 90.6%). The seed crystal used in the above was obtained by the method of the above example 5 without adding a seed crystal as the method of the above Example 5. Purity: 94.81% (HPLC)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865896B2
Source datasetuspto-grants-2014_10
ORD IDord-beb3253802a940acbfc61d2df5d93aa8
Source noteuspto-grants-2014_10