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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219467Generated: October 26, 2026

Potassium Carbonate → 1-{3-Chloro-6-[3-(1,1-dioxo-thiomorpholin-4-yl)-propoxy]-5-[3-(4-fluoro-phenyl)-butoxy]-4-methoxy-2-methyl-phenyl}-ethanone

https://huagongshe.com/reaction/219467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 1,1-dioxo-1lambda6-thiomorpholine-4-carboxylateHCID 21949260—
Reactant1-{2-(3-Bromo-propoxy)-5-chloro-3-[3-(4-fluoro-phenyl)-butoxy]-4-methoxy-6-methyl-phenyl}-ethanoneHCID 59583501—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product1-{3-Chloro-5-[3-(4-fluoro-phenyl)-butoxy]-4-methoxy-2-methyl-6-[3-(1-oxo-thiomorpholin-4-yl)-propoxy]-phenyl}-ethanoneHCID 2525468213%
Product1-{3-Chloro-6-[3-(1,1-dioxo-thiomorpholin-4-yl)-propoxy]-5-[3-(4-fluoro-phenyl)-butoxy]-4-methoxy-2-methyl-phenyl}-ethanoneHCID 2525468314%

Reaction Steps

A solution of N—BOC-1,1-dioxothiomorpholine (85 mg, 0.365 mmol) in a mixture of DCM (1 mL) and TFA (1 mL) was stirred at room temperature for 0.1 h before concentrating under vacuum and drying the TFA salt of 1,1-dioxothiomorpholine on the high vacuum pump for 3 h. The salt was dissolved in dry DMF (1 mL) and reacted with Example 22a (92 mg, 0.18 mmol) and K2CO3 (2.16 eq.) under General Procedure L. The crude mixture was purified by flash chromatography (silica gel, hexane/Et2O 1:4→MeOH/DCM 1:19) to afford 23 (14 mg, 14%) and 24 (13 mg, 13%) as clear colourless oils.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202513B2
Source datasetuspto-grants-2012_06
ORD IDord-d89ead20c28b4d1fb0e0ab5a5bfe7154
Source noteuspto-grants-2012_06