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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255260Generated: October 31, 2026

Sodium borohydride → HCID 15982019, compound

https://huagongshe.com/reaction/255260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15981895HCID 15981895—
SolventMethanolHCID 887—
ProductHCID 15982019HCID 15982019—

Reaction Steps

6-[({1-[2-(6-Acetyl-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl}amino)methyl]-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one (Example 45) (309 mg, 0.645 mmol) was reduced with sodium borohydride (47 mg, 2 equivalents) in methanol (12 mL) at 0° C. After quenching the reaction with water, the reaction mixture was concentrated under reduced pressure and extracted with chloroform. The chloroform layer was washed with brine and dried over magnesium sulfate and concentrated to dryness to give the as an off-white solid, 202 mg (95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875715B2
Source datasetuspto-grants-2011_01
ORD IDord-bb199891f99a44fe9639e0256e4c1391
Source noteuspto-grants-2011_01