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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050867Generated: October 30, 2026

Methylamine → HCID 71575823, compound

https://huagongshe.com/reaction/1050867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 86703363HCID 86703363—
ProductHCID 71575823HCID 7157582385.5%

Reaction Steps

A methanolic solution of methylamine (10 mL) was added to 1-(4-fluoro-phenyl)-4-iodo-2-oxo-1,2-dihydro-pyridine-3-carboxylic acid [4-(2-acetylamino-pyridin-4-yloxy)-2,5-difluoro-phenyl]-amide (90 mg, 0.145 mmol) and the resultant mixture was stirred at 80° C. for 3 h. The mixture was concentrated to dryness and the crude product was recrystallized from MeOH to afford N-(4-((2-acetamidopyridin-4-yl)oxy)-2,5-difluorophenyl)-1-(4-fluorophenyl)-4-(methylamino)-2-oxo-1,2-dihydropyridine-3-carboxamide (65 mg, 85.5% yield). 1H NMR (400 MHz, DMSO-d6): δ 13.21 (s, 1 H), 10.57 (s, 1 H), 10.34 (m, 1 H), 8.47 (dd, J=13.0, 7.2 Hz, 1 H), 8.17 (d, J=5.8 Hz, 1 H), 7.72 (d, J=7.8 Hz, 1 H), 7.65 (s, 1 H), 7.55-7.42 (m, 3 H), 7.33 (m, 2 H), 6.69 (d, J=5.9 Hz, 1 H), 6.24 (d, J=7.9 Hz, 1 H), 3.01 (d, J=5.0 Hz, 3 H), 2.02 (s, 3 H); MS (ESI) m/z: 524.01 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09387202B2
Source datasetuspto-grants-2016_07
ORD IDord-37daf6e05c6d4f359b994581d9d7a545
Source noteuspto-grants-2016_07