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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | 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 | HCID 77372940 | — |
| Product | 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 | HCID 57128234 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05162334 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-8df660c8fbdf4259909e62180a5b05ee |
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| Source note | uspto-grants-1992_11 |
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