Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621266Generated: November 2, 2026

Water → 2-((4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(5-methylisoxazol-3-yl)acetamide

https://huagongshe.com/reaction/1621266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,1-DichloroethaneHCID 6365—
Reactant3-Amino-5-methylisoxazoleHCID 66172—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium HexafluorophosphateHCID 2736652—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant2-((4,6-difluoro-1H-indol-3-yl)thio)acetic acidHCID 68003916—
SolventMethanolHCID 887—
Product2-((4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(5-methylisoxazol-3-yl)acetamideHCID 6800407826%

Reaction Steps

2-((4,6-difluoro-1H-indol-3-yl)thio)acetic acid (160 mg, 0.66 mmol) from Step B, 3-amino-5-methyl-isoxazole (130 mg, 1.32 mmol), PyClu (440 mg, 1.32 mmol), and DIEA (289 μL, 1.65 mmol) were added to dichloroethane (5 mL) and microwave irradiated at 110° C. for 30 minutes. The solvent was removed in vacuo and the remaining residue was dissolved in 5 mL (9:1, methanol:water) and oxone (641 mg, 1.0 mmol) was added and this mixture was stirred at ambient temperature overnight. Water (5 mL) was added and the mixture extracted with ethyl acetate (3×3 mL). The organics were combined, dried over magnesium sulfate, and concentrated in vacuo to give an oily residue which was purified on a silica gel column (0-50% ethyl acetate:hexanes over 19 min) to yield the desired product (62.0 mg, 0.174 mmol, 26% yield over 2 steps). LCMS>99% at 220 nm, RT=1.15 min, m/z=356 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772509B2
Source datasetuspto-grants-2014_07
ORD IDord-115b1c33249e4ed2b3fdc188196fe7f4
Source noteuspto-grants-2014_07