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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500396Generated: October 29, 2026

4-Cyanobenzoyl chloride → HCID 72445382, compound

https://huagongshe.com/reaction/500396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzoyl chlorideHCID 80172—
Reactanttert-butyl N-[4-(cyclopropylsulfonylcarbamoyl)-18-hydroxy-2,15-dioxo-3,16-diazatricyclo[14.3.0.04,6]nonadec-7-en-14-yl]carbamateHCID 68797769—
ProductHCID 72445382HCID 7244538237%

Reaction Steps

Prepared by way of method II using 18-hydroxy-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diazatricyclo[14.3.0.04,6]-nonadec-7-ene (100 mg, 0.175 mmol) and 4-cyanobenzoyl chloride (87 mg, 0.53 mmol). The final trituration (diethyl ether/hexane) and filtration gave 45 mg (37%) of 18-(4-cyanobenzoyloxy)-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diazatricyclo-[14.3.0.04,6]-nonadec-7-ene as a white powder: 99.0% pure (HPLC), MS m/z 696 (M−H)−, HRMS: calcd. 715.3125 and found 715.3147 (M+NH4)+, mp 164-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772183B2
Source datasetuspto-grants-2010_08
ORD IDord-37466a7e89d34ebd8aac580903b6c3c3
Source noteuspto-grants-2010_08