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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893202Generated: October 31, 2026

3-Fluoro-4-methylbenzylamine → Racemic-trans-n-(2-{[(3-fluoro-4-methylbenzyl)amino]carbonyl}-3-hydroxy-6-methyl-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepin-10-yl)-n,n',n'-trimethylethanediamide

https://huagongshe.com/reaction/1893202

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-methylbenzylamineHCID 2774597—
Reactanttrans-Rac-methyl 10-[[(dimethylamino)(oxo)acetyl](methyl)amino]-6-methyl-3-[(methylsulfonyl)oxy]-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepine-2-carboxylateHCID 87535816—
SolventDimethyl SulfoxideHCID 679—
ProductRacemic-trans-n-(2-{[(3-fluoro-4-methylbenzyl)amino]carbonyl}-3-hydroxy-6-methyl-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepin-10-yl)-n,n',n'-trimethylethanediamideHCID 54748167—

Reaction Conditions

Temperature100 °C

Reaction Steps

The trans-rac-methyl 10-[[(dimethylamino)(oxo)acetyl](methyl)amino]-6-methyl-3-[(methylsulfonyl)oxy]-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepine-2-carboxylate from Step 10 (50 mg) was dissolved in DMSO (2 mL) and 4-methyl-3-fluorobenzylamine (0.1 mL) added. The resulting mixture was heated at 100° C. for 30 minutes. As determined by LC-MS, there was complete conversion to product which was purified by reverse phase Gilson chromatography: 1H NMR (400 MHz, CDCl3) δ 9.46 (br s, 1H), 7.05 (m, 3H), 5.96 (m, 1H), 5.56 (br s, 1H), 4.47 (qd, J=6.8, 14.5 Hz, 2H), 3.02 (s, 3H), 2.99 (s, 3H), 2.94 (s, 3H), 2.21 (s, 3H), 1.61-2.24 (m, 6H), 1.47 (d, J=7.5 Hz, 3H). ES MS M+1=487.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513234B2
Source datasetuspto-grants-2013_08
ORD IDord-723bcfc8618b47139502242504f97bc1
Source noteuspto-grants-2013_08