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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708484Generated: October 28, 2026

1,1'-Carbonyldiimidazole → benzhydryl 1-[(Z)-[1-[2-[(2-methylpropan-2-yl)oxycarbonylamino]-1,3-thiazol-4-yl]-2-oxo-2-[[(3S,4R)-2-oxo-4-[(2-oxoimidazolidin-1-yl)methyl]azetidin-3-yl]amino]ethylidene]amino]oxycyclopropane-1-carboxylate

https://huagongshe.com/reaction/708484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactantbenzhydryl 1-[(Z)-[2-[[(2R,3S)-2-[(2-aminoethylamino)methyl]-4-oxoazetidin-3-yl]amino]-1-[2-[(2-methylpropan-2-yl)oxycarbonylamino]-1,3-thiazol-4-yl]-2-oxoethylidene]amino]oxycyclopropane-1-carboxylateHCID 118379472—
SolventChloroformHCID 6212—
Productbenzhydryl 1-[(Z)-[1-[2-[(2-methylpropan-2-yl)oxycarbonylamino]-1,3-thiazol-4-yl]-2-oxo-2-[[(3S,4R)-2-oxo-4-[(2-oxoimidazolidin-1-yl)methyl]azetidin-3-yl]amino]ethylidene]amino]oxycyclopropane-1-carboxylateHCID 11838023549.1%

Reaction Steps

To a solution of benzhydryl 1-(((Z)-(2-(((2R,3S)-2-(((2-aminoethyl)amino)methyl)-4-oxoazetidin-3-yl)amino)-1-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)-2-oxoethylidene)amino)oxy)cyclopropanecarboxylate (90 mg, 0.133 mmol) in chloroform (2.7 mL) was added CDI (43.1 mg, 0.266 mmol) and TEA (111 μl, 0.797 mmol). After 12 h, the reaction mixture was concentrated in vacuo. The crude residue was purified via silica gel chromatography (MeOH-DCM, 0-100%) to afford the title compound (46 mg, 49%). LCMS: Rt=0.95 min, m/z=704.0 (M+1), Method 2m_acidic.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-27cc3506b2094d95aa07f5ff1d1e0285
Source noteuspto-grants-2015_11