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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082624Generated: November 2, 2026

2-Nitrobenzenesulfonyl chloride → HCID 57303972, compound

https://huagongshe.com/reaction/2082624

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57280761HCID 57280761—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 57303972HCID 57303972—

Reaction Steps

To a solution of 17-ethyl-20-fluoro-1-hydroxy-12-[2'-(3",4"-dihydroxycyclohexyl)-1'-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-aza-tricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone (200 mg) in dry methylene chloride (20 ml) is added diisopropylethylamine (150 μl) followed by 2-nitrobenzenesulonyl chloride (60 mg), then 4-dimethylaminopyridine (27 mg). The solution is stirred at room temperature under nitrogen atmosphere for 4 h, then quenched with sat'd aqueous sodium bicarbonate solution. The organic layer is washed (water, sat'd NaHCO3, sat'd NaCl), dried (anhydrous Na2SO4) and the solvent is removed in vacuo. Chromatography on silica gel gives the title compounds.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189042
Source datasetuspto-grants-1993_02
ORD IDord-44ea22049a0a41c8a5e17bc506f74c47
Source noteuspto-grants-1993_02