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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646206Generated: October 30, 2026

1,1'-Carbonyldiimidazole → HCID 25007954, compound

https://huagongshe.com/reaction/646206

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 23614307HCID 23614307—
ReactantHCID 59264602HCID 59264602—
SolventDimethylacetamideHCID 31374—
ProductHCID 25007954HCID 2500795444.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of [2-[2-(2,3-difluorophenyl)ethyl]-4-oxo-1,8-naphthyridin-1(4H)-yl]acetic acid (Int. C2) (100 mg, 1 equiv), carbonyldiimidazole (50 mg, 1.05 equiv) and dimethyl-acetamide (4 ml) was stirred at 60° C. for 30 min then methyl 2-methyl-2-[4-({[4′-(trifluoro-methyl)-4-biphenylyl]methyl}amino)-1-piperidinyl]propanoate (Int. B1) (132 mg, 1.05 equiv) was added and the temperature raised to 80° C. for 2 h. A further portion of carbonyldiimidazole (0.5 equiv) was added and stirring continued at 80° C. for 15 h. After cooling the crude mixture was applied to reverse phase HPLC (Preparative Method A) to obtain methyl 2-[4-({[2-[2-(2,3-difluorophenyl)ethyl]-4-oxo-1,8-naphthyridin-1(4H)-yl]-acetyl} {[4′-(trifluoromethyl)-4-biphenylyl]methyl}amino)-1-piperidinyl]-2-methyl-propanoate (99 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705005B2
Source datasetuspto-grants-2010_04
ORD IDord-2b62a205938040f89efb64519af1eec8
Source noteuspto-grants-2010_04