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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242271Generated: October 31, 2026

HCID 86644984, compound → HCID 66782422, compound

https://huagongshe.com/reaction/2242271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86644984HCID 86644984—
SolventFormic AcidHCID 284—
ProductHCID 66782422HCID 6678242244.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671054B1
Source datasetuspto-grants-2010_03
ORD IDord-7f66b742afb34c7e87f386e505aa05f5
Source noteuspto-grants-2010_03