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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417224Generated: November 3, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 140397795, compound

https://huagongshe.com/reaction/1417224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 54425842HCID 54425842—
ReactantHCID 140397783HCID 140397783—
SolventDimethylformamideHCID 6228—
ProductHCID 140397795HCID 14039779551.8%

Reaction Steps

In 7.5 ml of N,N-dimethylformamide was dissolved 2.5 g of 4-[3-(4-tert-butoxycarbonylamidinophenoxy) propyl]-2,3-dioxopiperazine, and to the solution were added 6.1 g of diphenylmethyl 3-(3-pyridyl)acrylate and 0.48 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene. The resulting mixture was stirred overnight at room temperature and distilled under reduced pressure to remove the solvent. To the resulting residue were added 80 ml of ethyl acetate and 60 ml of water and the pH was adjusted to 7 with 2N hydrochloric acid. The organic layer was separated, washed with water and then a saturated aqueous sodium chloride solution, and then distilled under reduced pressure to remove the solvent. The resulting residue was purified by a silica gel column chromatography (eluent; chloroform: methanol=20:1) to obtain 2.34 g of diphenylmethyl 3-[4-[3-(4-tert -butoxycarbonylamidinophenoxy)propyl]-2,3-dioxopiperazin-1-yl]-3-(pyridin-3-yl)propionate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877174
Source datasetuspto-grants-1999_03
ORD IDord-9fe341cf84dc4ab498d4c4c2853e8e02
Source noteuspto-grants-1999_03