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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354205Generated: November 1, 2026

Sodium borohydride → HCID 21104611, compound

https://huagongshe.com/reaction/1354205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carbaldehydeHCID 10773638—
ReactantHCID 21104608HCID 21104608—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 21104611HCID 21104611—

Reaction Steps

Molecular sieve, type 3A, (1.082 g) and 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbaldehyde (0.095 g, 0.54 mmol) were added to a solution of (3S)-2-(3-aminomethyl-piperidin-1-yl)-1-(6-methoxy-quinolin-4-yl)-ethanol (0.171 g, 0.54 mmol) in MeOH (1.6 ml) and dichloromethane (3.8 ml). The reaction mixture was stirred at room temperature for 16 hours and sodium borohydride (0.054 g, 1.43 mmol) was added. The reaction mixture was stirred at room temperature for 2 hours and then filtered over Hydromatrix (wetted with an NaHCO3 solution, 2 ml) and subsequently washed with dichloromethane. The filtrate was concentrated to dryness by rotary evaporation. The residue was purified by column chromatography on silica gel (dichloromethane/MeOH 9/1 1% NH4OH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223776B2
Source datasetuspto-grants-2007_05
ORD IDord-5f38059a67f647dc8b1faf166a3e2dc7
Source noteuspto-grants-2007_05