Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226790Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 57233353, compound

https://huagongshe.com/reaction/2226790

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 131718679HCID 131718679—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 57233353HCID 5723335367.9%

Reaction Steps

To a solution of 17-ethyl-1,14-dihydroxy-12-[2'-(3"-hydroxy-4"-(1-t-butyl-dimethylsilyloxyethylindol-5-yl)oxycyclohexyl)-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 (74mg) in CH2Cl2 (2 mL.) at rt was added a solution of p-toluene sulfonic acid (10 mg.) in CH3OH (2 mL.). The reaction mixture was stirred for 3 hr., quenched with saturated NaHCO3, then extracted with CH2Cl2. The extracts were combined, dried over Na2SO4, filtered and concentrated in vacuo. The product was purified by preparative TLC on silica gel (2:1, hexane/acetone) to give 44.8 mg of the title compound. Partial 1H NMR (CDCl, 200 MHz) d: 7.24 (d, J=9 Hz, 1H); 7.15 (d, J=3 Hz, 1H); 7.12 (d, J=3.5 Hz, 1H); 6.86 (dd, J=3 and J=9 Hz, 1H); 6.39 (d, J=3.5, 1H); 4.20 (t, J=5, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05349061
Source datasetuspto-grants-1994_09
ORD IDord-a4de34babb2b4c53acf9254a80123db0
Source noteuspto-grants-1994_09