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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358654Generated: November 1, 2026

2-(4-Methoxy-phenylsulfanyl)-5-methyl-phenylamine → [2-(4-Methoxy-phenylsulfanyl)-5-methyl-phenyl]-(7-propyl-[1,8]naphthyridin-4-yl)-amine

https://huagongshe.com/reaction/2358654

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Methoxy-phenylsulfanyl)-5-methyl-phenylamineHCID 43349616—
Reactant5-Chloro-2-propyl-[1,8]naphthyridineHCID 44140176—
Product[2-(4-Methoxy-phenylsulfanyl)-5-methyl-phenyl]-(7-propyl-[1,8]naphthyridin-4-yl)-amineHCID 68460687—

Reaction Steps

The product from Example 2g (275 mg, 1.33 mmol) was reacted with the product from Example 50b (326 mg, 1.33 mmol) for 18 h following the procedure from Example 1g giving the crude title compound which was purified by HPLC with TFA providing the product as a trifluoroacetic acid (392 mg, 56%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 0.98 (t, J=7.35 Hz, 3 H) 1.85 (m, 2 H) 2.34 (s, 3 H) 3.00 (t, J=7.54 Hz, 2 H) 3.72 (s, 3 H) 6.27 (d, J=6.99 Hz, 1 H) 6.84 (d, J=8.82 Hz, 2 H) 7.11 (d, J=7.72 Hz, 1 H) 7.27 (m, 4 H) 7.83 (d, J=8.82 Hz, 1 H) 8.41 (d, J=6.99 Hz, 1H) 9.02 (d, J=8.46 Hz, 1 H) 11.06 (br. s., 1 H) 14.37 (br. s., 1 H); MS (ESI+) m/z 416 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763731B2
Source datasetuspto-grants-2010_07
ORD IDord-2606dadb46314b81a6f0f04238179c3b
Source noteuspto-grants-2010_07