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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986083Generated: November 1, 2026

2-Fluoro-N-(4-fluorobenzyl)nicotinamide → 2-(4-(1h-Pyrrolo[2,3-b]pyridin-4-yloxy)-3-fluorophenylamino)-n-(4-fluorobenzyl)nicotinamide, dihydrochloride salt

https://huagongshe.com/reaction/1986083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-N-(4-fluorobenzyl)nicotinamideHCID 57721335—
Reactant2-(4-(1H-Pyrrolo[2,3-b]pyridin-4-yloxy)-3-fluorophenylamino)-N-o-tolylnicotinamide, dihydrochloride saltHCID 131727483—
Product2-(4-(1h-Pyrrolo[2,3-b]pyridin-4-yloxy)-3-fluorophenylamino)-n-(4-fluorobenzyl)nicotinamide, dihydrochloride saltHCID 13172748635%

Reaction Steps

2-Fluoro-N-(4-fluorobenzyl)nicotinamide (0.050 g, 0.20 mmol) was converted to the title compound (0.035 g, 35%) in a manner similar to the preparation of 2-(4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)-3-fluorophenylamino)-N-o-tolylnicotinamide (Step B of Example 8). 1H NMR (DMSO-d6) δ 12.63 (s, 1H), 11.17 (s, 1H), 9.44 (t, 1H, J=5.8 Hz), 8.10-8.40 (m, 4H), 7.50-7.60 (m, 1H), 7.30-7.45 (m, 4H), 7.08-7.10 (m, 2H), 6.90-6.95 (m, 1H), 6.66 (d, 1H, J=6.3 Hz), 6.43-6.46 (m, 1H), 4.44 (d, 2H, J=5.7 Hz); HRMS(ESI+), 472.1585 (M+H)+ calc, 472.1587 (M+H)+ found.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547782B2
Source datasetuspto-grants-2009_06
ORD IDord-0b057009c56141bd97ff35012cafa2e5
Source noteuspto-grants-2009_06