HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554722Generated: October 30, 2026
HCID 86644984, compound → HCID 66782422, compound
https://huagongshe.com/reaction/554722
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86644984 | HCID 86644984 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 66782422 | HCID 66782422 | 44.1% |
Reaction Steps
A solution of crude 3-(3-Benzyl-ureido)-hex-5-enoic acid [1-[benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-amine (3.26 g, 4.95 mmol) in formic acid (100 mL) was stirred at room temperature for 13 h. The solvent was removed under reduced pressure and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na2SO4 and concentrated in vacuo. The residue was purified by chromatography and recrystallized on ethyl acetate and hexane to give the 8-Benzyl-6-(4-hydroxy-benzyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide (1.12 g, 3 step yield: 38%), 1H NMR (CDCl3, 300 MHz) δ 7.5˜7.3 (m, 5H), 7.2 (d, J=7.01, 2H), 6.80 (m, 5H), 6.5 (d, J=8.76, 2H), 5.6 (m, 1H), 5.25 (t, J=4.7, 1H), 4.55 (m, 1H), 4.5˜4.25 (m, 4H, OH), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H) 2.2 (t, J=7.2, 2H) 1.36 (m, 3H) MS ESI 513(M+H), 535 (M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08049008B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-51d6e2eb5a6649bf8468ecc11c948d26 |
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| Source note | uspto-grants-2011_11 |
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