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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500387Generated: October 25, 2026

4-Phenoxybenzoyl chloride → 18-(4-Phenoxybenzoyloxy)-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diaza-12-oxatricyclo-[14.3.0.04,6]-nonadec-7-ene

https://huagongshe.com/reaction/500387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenoxybenzoyl chlorideHCID 74193—
Reactant18-Hydroxy-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diaza-12-oxatricyclo[14.3.0.04,6]-nonadec-7-eneHCID 72260127—
Product18-(4-Phenoxybenzoyloxy)-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diaza-12-oxatricyclo-[14.3.0.04,6]-nonadec-7-eneHCID 7244537912%

Reaction Steps

Prepared by way of method I using 18-hydroxy-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diaza-12-oxatricyclo[14.3.0.04,6]-nonadec-7-ene (100 mg, 0.175 mmol) and 4-phenoxybenzoyl chloride (111 mg, 0.53 mmol). The final trituration (diethyl ether/hexane) and filtration gave 16 mg (12%) of 18-(4-phenoxybenzoyloxy)-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diaza-12-oxatricyclo-[14.3.0.04,6]-nonadec-7-ene as a white powder: 97.5% pure (HPLC), MS m/z 765 (M−H)−, HRMS: calcd. 784.3228 and found 784.3208 (M+NH4)+, mp 207-209° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772183B2
Source datasetuspto-grants-2010_08
ORD IDord-1e1e4a6e0a1446e58ef67db394875462
Source noteuspto-grants-2010_08