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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350914Generated: October 25, 2026

Glycinamide hydrochloride → 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-4-methyl-N-{1-[(methylamino)carbonyl]methyl}benzamide

https://huagongshe.com/reaction/350914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycinamide hydrochlorideHCID 2723639—
Reactant3-[5-chloro-4-[(2,4-difluorobenzyl)oxy)-6-oxopyrimidin-1(6H)-yl]-N-[1-(aminocarbonyl)methyl]-4-methylbenzamideHCID 21089008—
Product3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-4-methyl-N-{1-[(methylamino)carbonyl]methyl}benzamideHCID 21089007—

Reaction Steps

The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis of 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-[1-(aminocarbonyl)methyl]-4-methylbenzamide by substituting glycine methyl amide HCl for glycineamide HCl. 1H NMR (CD3OD/400 MHz) δ8.32 (s, 1H), 7.96 (m, 1H), 7.81 (s, 1H), 7.61 (q, 1H, J=8.4 Hz), 7.55 (d, 1H, J=8.0 Hz), 7.02 (m, 2H), 5.60 (m, 2H), 3.99 (s, 2H), 2.74 (s, 3H), 2.21 (s, 3H). ESHRMS m/z 477.1141 (M+H calculated for C22H20ClF2N4O4 requires 477.1136).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183287B2
Source datasetuspto-grants-2007_02
ORD IDord-7ef091929f0f44318d17017114ed7c24
Source noteuspto-grants-2007_02