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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Fluoro-4-methylbenzylamine | HCID 2774597 | — |
| Reactant | 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 | HCID 87535816 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 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 | HCID 54748167 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513234B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-723bcfc8618b47139502242504f97bc1 |
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| Source note | uspto-grants-2013_08 |
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