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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476362Generated: October 29, 2026

N-[4-(4-amino-2,5-difluorophenoxy)-6-chloropyrimidin-2-yl]acetamide → N-[4-(4-amino-2,5-difluorophenoxy)pyrimidin-2-yl]acetamide

https://huagongshe.com/reaction/476362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(4-amino-2,5-difluorophenoxy)-6-chloropyrimidin-2-yl]acetamideHCID 86662870—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-[4-(4-amino-2,5-difluorophenoxy)pyrimidin-2-yl]acetamideHCID 6660496682%

Reaction Conditions

Temperature15 °C

Reaction Steps

A mixture of N-[4-(4-amino-2,5-difluoro-phenoxy)-6-chloro-pyrimidin-2-yl]-acetamide (3.3 g, 10.5 mmol) and palladium on carbon (1.0 g, 10%) in methanol (100 mL) was stirred under H2 (1 atm) at 15° C. for 4 h. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure to give N-[4-(4-amino-2,5-difluoro-phenoxy)-pyrimidin-2-yl]-acetamide (2.4 g, 82% yield) as a pale yellow solid. 1HNMR (400 MHz, DMSO-d6): δ10.37 (s, 1H), 8.44 (d, J=5.7 Hz, 1H), 7.15 (dd, J=11.4 Hz, J=4.8 Hz, 1H) 6.71 (d, J=5.7 Hz, 1H), 6.65 (dd. J=12.3 Hz, J=8.4 Hz, 1H), 5.40 (s, 2H), 1.99 (s, 3H); MS (ESI) m/z: 281.2[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637672B2
Source datasetuspto-grants-2014_01
ORD IDord-2ca6a29cbc5741bebde07e165db9588d
Source noteuspto-grants-2014_01