HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373276Generated: October 31, 2026
2-Nitrobenzenesulfonyl chloride → HCID 57236676, compound
https://huagongshe.com/reaction/373276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 56989260 | HCID 56989260 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57236676 | HCID 57236676 | 81.2% |
Reaction Steps
To a solution of 17-ethyl-1-hydroxy-12-[2'-(4"-hydroxy-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 (66 mg) in dry methylene chloride (1.4 ml) was added an excess of diisopropylethyl amine (34 μl) and o-nitrobenzenesulfonyl chloride (36 mg) followed by addition of 4-dimethylaminopyridine (24 mg). The mixture was stirred at room temperature for 18 hours at which time it was diluted with ethyl acetate, extracted from saturated sodium bicarbonate solution and washed with brine. The combined organics were dried over magnesium sulfate and the concentrate purified by flash chromatography on silica gel (ethyl acetate:hexane (1:1)+1% methanol to give the title compound (66 mg).
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-f9936379984a48b6ac5a823cbd1c3a48 |
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| Source note | uspto-grants-1992_11 |
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