Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414804Generated: November 1, 2026

Acetic Anhydride → HCID 22643590, compound

https://huagongshe.com/reaction/2414804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 22643561HCID 22643561—
SolventAcetonitrileHCID 6342—
ProductHCID 22643590HCID 2264359078%

Reaction Steps

The 2-amino-N-[[4-(5-methyl-3-phenylisoxazol-4-yl)phenyl]sulfonyl]acetamide (Example 81)(4.08 g, 10.9 mmol) was mixed in acetonitrile at room temperature. Triethylamine (3.03 g, 30.0 mmol) and acetic anhydride (1.23 g, 12.1 mmol) were added and the heterogeneous solution was stirred for 2 hours. The solution was vacuum filtered through a pad of diatomaceous earth and solvent was removed at reduced pressure. Water was added and the solution was stirred for 30 minutes. White crystals formed, were collected by vacuum filtration and dried to afford the desired product as a white solid (3.25 g, 78%): mp 218.2-219.3° C. 1H NMR (CD3OD/300 MHz) 8.01 (d, 2H, J=8.2 Hz), 7.42-7.36 (m, 7H), 3.85 (s, 2H), 2.50 (s, 3H), 1.95 (s, 3H). FABLRMS m/z 414 (M+H). Anal. Calc'd for C20H19N3O5S: C, 58.10; H, 4.63; N,10.16. Found: C, 58.18; H, 4.66; N, 10.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815460B2
Source datasetuspto-grants-2004_11
ORD IDord-2b02e9a6e17242e5976eb76daef94da1
Source noteuspto-grants-2004_11