HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373544Generated: October 31, 2026
Sodium borohydride → HCID 21073762, compound
https://huagongshe.com/reaction/1373544
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21073768 | HCID 21073768 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21073762 | HCID 21073762 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160888B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-c597855a344b495e8f061e3540119404 |
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| Source note | uspto-grants-2007_01 |
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