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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390815Generated: October 29, 2026

Pyridine → HCID 67069936, compound

https://huagongshe.com/reaction/2390815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 67069927HCID 67069927—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 67069936HCID 6706993646%

Reaction Steps

step 6—To solution of 88 (0.087 g, 0.19 mmol) in DCM (5 mL) at 0° C. was added pyridine (23 □L) and followed by acetic anhydride (0.02 mL, 0.23 mmol). The reaction was allowed to warm to RT and stirred overnight then diluted with DCM and saturated aqueous NaHCO3. The aqueous layer was separated and extracted with DCM. The combined extract was washed with brine, dried (Na2SO4), filtered and concentrated. The crude product was purified on a preparative SiO2 TLC plate developed with 40% EtOAc/hexanes to afford 0.045 g (46%) of N-[4-tert-butyl-2-[2-(4-methanesulfonylamino-phenyl)-ethyl]-6-(2-methoxy-pyridin-3-yl)-phenyl]-acetamide (90) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273773B2
Source datasetuspto-grants-2012_09
ORD IDord-aa40ba0a788d455ca3832a954184d613
Source noteuspto-grants-2012_09