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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358572Generated: November 4, 2026

Sodium borohydride → N-(4-{2-[7-(2-Hydroxy-ethyl)-[1,8]naphthyridin-4-ylamino]-4-methyl-phenylsulfanyl}-phenyl)-acetamide

https://huagongshe.com/reaction/2358572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-{5-[2-(4-Acetylamino-phenylsulfanyl)-5-methyl-phenylamino]-[1,8]naphthyridin-2-yl}-malonic acid diethyl esterHCID 67250853—
SolventEthanolHCID 702—
ProductN-(4-{2-[7-(2-Hydroxy-ethyl)-[1,8]naphthyridin-4-ylamino]-4-methyl-phenylsulfanyl}-phenyl)-acetamideHCID 24898183—

Reaction Steps

The product from Example 24b (56 mg, 0.10 mmol) was reacted with NaBH4 (40 mg, 1.00 mmol) in 5 mL EtOH for 24 h. Quenched with aqueous NH4Cl and adjusted to pH 7 with dilute HCl. Extracted with EtOAc and dried over Na2SO4, filtered and concentrated under vacuum giving the crude title compound which was purified by HPLC with TFA giving the trifluoroacetic acid salt (15 mg, 25%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 2.04 (s, 3H) 2.35 (s, 3H) 3.16 (t, J=6.43 Hz, 2H) 3.91 (t, J=6.25 Hz, 2H) 6.31 (d, J=6.99 Hz, 1H) 7.14 (d, J=8.09 Hz, 1H) 7.22-7.33 (m, 4H) 7.51 (d, J=8.82 Hz, 2H) 7.83 (d, J=8.82 Hz, 1H) 8.42 (d, J=6.99 Hz, 1H) 8.94-9.05 (m, 1H) 10.04 (s, 1H) 11.03 (s, 1H) 14.40 (s, 1H); MS (ESI+) m/z 445 (M+H−TFA)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763731B2
Source datasetuspto-grants-2010_07
ORD IDord-1c1ceaf64c7e47118dcdfafd463cb8c3
Source noteuspto-grants-2010_07