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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281725Generated: October 26, 2026

N-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamide → N-{3-[3-(1-tert-butoxycarbonylpyrrolidin-3-yloxy)benzamido]-4-methylphenyl}-2-morpholinopyridine-4-carboxamide

https://huagongshe.com/reaction/1281725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamideHCID 17904941—
Reactant3-{[1-(tert-Butoxycarbonyl)pyrrolidin-3-yl]oxy}benzoic acidHCID 22291136—
ProductN-{3-[3-(1-tert-butoxycarbonylpyrrolidin-3-yloxy)benzamido]-4-methylphenyl}-2-morpholinopyridine-4-carboxamideHCID 18422094—

Reaction Steps

Using an analogous procedure to that described in the first paragraph of Example 26, 3-(1-tert-butoxycarbonylpyrrolidin-3-yloxy)benzoic acid was reacted with N-(3-amino4-methylphenyl)-2-morpholinopyridine4-carboxamide to give N-{3-[3-(1-tert-butoxycarbonylpyrrolidin-3-yloxy)benzamido]-4-methylphenyl}-2-morpholinopyridine-4-carboxamide; NMR Spectrum: (DMSOd6) 1.42 (s, 9H), 2.15 (s, 2H), 2.22 (s, 3H), 3.44 (m, 3H), 3.55 (t, 4H), 3.6 (m, 1H), 3.77 (t, 4H), 5.18 (m, 1H), 7.13 (d, 1H), 7.21 (m, 1H), 7.37 (m, 2H), 7.5 (t, 1H), 7.56 (s, 1H), 7.61 (d, 2H), 7.81 (d, 1H), 8.3 (d, 1H), 9.9 (s, 1H), 10.31 (s, 1H); Mass Spectrum: M+H+ 602.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455520B1
Source datasetuspto-grants-2002_09
ORD IDord-de700c03cc0046c3bfad9327945be474
Source noteuspto-grants-2002_09