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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500391Generated: October 31, 2026

p-Anisoyl chloride → HCID 72445402, compound

https://huagongshe.com/reaction/500391

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
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 72445402HCID 7244540227%

Reaction Steps

Prepared by way of method I 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-methoxybenzoyl chloride (72 mg, 0.53 mmol). The final trituration (diethyl ether/hexane) and filtration gave 33 mg (27%) of 18-(4-methoxybenzoyloxy)-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diazatricyclo-[14.3.0.04,6]-nonadec-7-ene as a white powder: 98.0% pure (HPLC), MS m/z 701 (M−H)−, HRMS: calcd. 703.3013 and found 703.3006 (M+H)+, mp 151-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772183B2
Source datasetuspto-grants-2010_08
ORD IDord-595986589d204be49c523a03ad05cfaa
Source noteuspto-grants-2010_08