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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271692Generated: November 2, 2026

Sodium Sulfate → HCID 10114705, compound

https://huagongshe.com/reaction/1271692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantSodium borohydrideHCID 4311764—
Reactant5,6,7,8-Tetrahydro-1,8-naphthyridine-2-carbaldehydeHCID 21873725—
ReactantHCID 23400257HCID 23400257—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 10114705HCID 1011470583%

Reaction Steps

To a stirred solution of (R)-2-(4-aminopiperidin-1-yl)-1-(6-methoxy-[1,5]naphthyridin-4-yl)ethanol (2f) (0.30 g, 1.0 mmole) in CH2Cl2 (25 mL) and dry ethanol (10 mL) at RT was added 5,6,7,8-tetrahydro-[1,8]naphthyridine-2-carboxaldehyde (prepared according to the procedure of WO 98/08840, 0.17 g, 1.0 mmole) and granular Na2SO4 (approximately 200 mg). After 36 h, the reaction was filtered through a sintered-glass funnel and the filtrate was concentrated. The remaining residue was dissolved in dry ethanol and reacted with NaBH4 (0.04 g, 1.0 mmole). After 12 h at RT, the reaction was concentrated under vacuum and the residue was dissolved in a mixture of H2O (2 mL) and saturated aqueous NaHCO3 (10 mL). The aqueous solution was extracted with EtOAc (2×50 mL) and the combined organic phases were washed with brine then were dried over Na2SO4. Flash chromatography on silica gel (9:1 CHCl3/MeOH containing 5% NH4OH) afforded the title compound (0.37 g, 83%) as a white solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205408B2
Source datasetuspto-grants-2007_04
ORD IDord-36370233f60d4fdc985a07c29a0f5fde
Source noteuspto-grants-2007_04