HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226782Generated: November 2, 2026
HCID 57154952, compound → HCID 56989260, compound
https://huagongshe.com/reaction/2226782
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57154952 | HCID 57154952 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 56989260 | HCID 56989260 | 41.7% |
Reaction Steps
To a solution of 17-ethyl-1-hydroxy-12-[2'-(4"-(tert-butyldimethylsiloxy)-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 (115 mg) (STEP 31A) in acetonitrile (2.5 ml) was added a solution of 2% HF in aqueous acetonitrile (40 μl), and the mixture was stirred at room temperature. After 4 hours, the solution was diluted with ethyl acetate and quenched with saturated sodium bicarbonate. The layers were separated, and the organic layer was washed with brine and dried over magnesium sulfate. Purification of the concentrate-by flash chromatography on silica gel (ethyl acetate:hexane (1:2)) gave the title compound (42 mg). 1H NMR consistent with the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05349061 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-a6138447172743f39c4dca7727e7ecf3 |
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| Source note | uspto-grants-1994_09 |
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