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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644379Generated: November 1, 2026

Sodium borohydride → HCID 15982019, compound

https://huagongshe.com/reaction/1644379

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 numberUS08124602B2
Source datasetuspto-grants-2012_02
ORD IDord-08755f304c1f4ed6add359102ffb866a
Source noteuspto-grants-2012_02