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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935428Generated: November 3, 2026

Pyridine → HCID 22999712, compound

https://huagongshe.com/reaction/1935428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 22999703HCID 22999703—
SolventDichloromethaneHCID 6344—
ProductHCID 22999712HCID 22999712—

Reaction Steps

To a stirring solution of 2-{[5-({[4-(tert-butyl)phenyl]sulfonyl}amino)-4-iodo-3-isoxazolyl]oxy}ethyl acetate (Preparation 4) (9.44 g) in dichloromethane was added pyridine (1.65 mL) followed by the slow addition of isobutylchloroforomate (2.41 mL) over 10 minutes. The reaction mixture was stirred at room temperature for one hour. The solvent was removed in vacuo to yield the crude material. This was purified using column chromatography (300 g silica, compound loaded with dichloromethane (15 mL) using a gradient elution of hexane (100% to 75%) and ethyl acetate (0% to 25%) to yield the desired compound as a yellow oil (7.70 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387915B2
Source datasetuspto-grants-2002_05
ORD IDord-338982eabc6640639445d54445b7c667
Source noteuspto-grants-2002_05