Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373544Generated: October 31, 2026

Sodium borohydride → HCID 21073762, compound

https://huagongshe.com/reaction/1373544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21073768HCID 21073768—
SolventMethanolHCID 887—
ProductHCID 21073762HCID 2107376267%

Reaction Steps

To a solution of 7-{4-[4-(7-oxo-5,6,7,8-tetrahydro-naphthalen-1-yl)-piperazin-1-yl]-butoxy}-3,4-dihydro-1H-[1,8]naphthyridin-2-one (0.24 g, 0.54 mmol) in methanol (5 mL) was added portionwise NaBH4 (0.081 g, 2.14 mmol). The reaction mixture was stirred at room temperature for 30 min and quenched with saturated NH4Cl solution and the compound was extracted with CH2Cl2 (2×20 mL). The organic layer was washed with brine (20 mL), dried over anhydrous Na2SO4, filtered and evaporated. The crude product was purified by column chromatography (10% methanol in ethyl acetate) to afford compound the title compound (0.16 g, 67%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.54 (s, 1H), 7.36 (d, 1H), 7.12 (t, 1H), 6.93–6.85 (m, 2H), 6.35 (d, 1H), 4.23 (t, 2H), 4.14–4.09 (m, 1H), 3.20–3.19 (m, 1H), 3.02–2.83 (m, 8H), 2.66–2.47 (m 10H), 1.83–1.67 (m, 6H). ES MS: 451.27 (M+H)+ (Exact mass: 450.26).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160888B2
Source datasetuspto-grants-2007_01
ORD IDord-c597855a344b495e8f061e3540119404
Source noteuspto-grants-2007_01