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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373281Generated: October 25, 2026

Methyl formate → 17-Ethyl-1-hydroxy-12-[2-(4"-formamido-3"-allyloxy-cyclohexyl)-1'-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo-[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetraone

https://huagongshe.com/reaction/373281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl formateHCID 7865—
Reactant17-Ethyl-1-hydroxy-12-[2'-(4 "-amino-3"-allyloxycyclohexyl)-1'-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetraoneHCID 77372940—
Product17-Ethyl-1-hydroxy-12-[2-(4"-formamido-3"-allyloxy-cyclohexyl)-1'-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo-[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetraoneHCID 57128234—

Reaction Conditions

Temperature0 °C

Reaction Steps

The compound 17-ethyl-1-hydroxy-12-[2'-(4"-amino-3"-allyloxycyclohexyl)-1'-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone (30 mg) is mixed with methyl formate (0.5 ml) and is stirred at 0° C. for 1 hr. The reaction mixture is allowed to warm to room temperature and then is stirred overnight. The excess methylformate is removed with nitrogen flow and the crude mixture is purified by preparative tlc on silica gel to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162334
Source datasetuspto-grants-1992_11
ORD IDord-8df660c8fbdf4259909e62180a5b05ee
Source noteuspto-grants-1992_11