HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554739Generated: October 28, 2026
HCID 66782407, compound → HCID 66782284, compound
https://huagongshe.com/reaction/554739
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 66782407 | HCID 66782407 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 66782284 | HCID 66782284 | 37.2% |
Reaction Steps
A solution of crude N-[1-[Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)ethyl]-3-(3-benzyl-ureido)-butyramide (3.55 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 8-Benzothiazol-4-ylmethyl-6-(4-hydroxy-benzyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide (1.05 g, 3 step yield: 32%). 1H NMR (CDCl3, 300 MHz) δ 9.25 (s, 1H), 7.4˜7.26 (m, 3H), 7.2 (d, J=7.01, 2H), 6.98 (t, J=8.0, 1H), 6.85 (m, 3H), 6.8 (t, J=7.0, 1H), 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), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H), 2.2 (t, J=7.2, 2H) 1.45 (m, 3H) MS ESI 570 (M+H), 592 (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-dea12dc0b19d4cf3a24e1b430f22cc7d |
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| Source note | uspto-grants-2011_11 |
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