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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641141Generated: November 1, 2026

1,3-Dioxolane-2-methanamine, N-methyl- → N-[4-({2-[(1,3-Dioxolan-2-ylmethyl)(methyl)amino]pyrimidin-4-yl}oxy)-1-naphthyl]-3-fluoro-5-morpholin-4-ylbenzamide

https://huagongshe.com/reaction/1641141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dioxolane-2-methanamine, N-methyl-HCID 541754—
Reactant3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamideHCID 59553095—
ProductN-[4-({2-[(1,3-Dioxolan-2-ylmethyl)(methyl)amino]pyrimidin-4-yl}oxy)-1-naphthyl]-3-fluoro-5-morpholin-4-ylbenzamideHCID 59553263—

Reaction Steps

Compound is prepared from 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide and [1,3]dioxolan-2-ylmethyl-methylamine according to conditions described in general procedure C. Mp: 111-112° C.; 1H NMR (400 MHz, DMSO-d6) δ 2.75-3.96 (m, 8H), 3.27 (m, 4H), 3.80 (m, 4H), 4.75-5.0 (m, 2H), 6.27 (d, J=5.1 Hz, 1H), 7.05 (d, J=12.5 Hz, 1H), 7.28 (d, J=8.8 Hz, 1H), 7.42-7.62 (m, 5H), 7.84 (d, J=7.7 Hz, 1H), 7.99-8.01 (m, 1H), 8.28 (d, J =5.5 Hz, 1H), 10.47 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114873B2
Source datasetuspto-grants-2012_02
ORD IDord-3fe8e545a11142f68208c4f5152138b4
Source noteuspto-grants-2012_02