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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766300Generated: October 26, 2026

Acetic Anhydride → N-acetyl-N-(5-amino-benzo[d]isothiazol-3-yl)-acetamide

https://huagongshe.com/reaction/1766300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant3-Amino-5-nitrobenzisothiazoleHCID 158638—
ReactantN-acetyl-N-(5-nitro-benzo[d]isothiazol-3-yl)-acetamideHCID 21110339—
SolventDimethylformamideHCID 6228—
ProductN-acetyl-N-(5-amino-benzo[d]isothiazol-3-yl)-acetamideHCID 21110338—

Reaction Steps

N-acetyl-N-(5-nitro-benzo[d]isothiazol-3-yl)-acetamide (KRB01049): To a solution of 3-amino-5-nitrobenzisothiazole (1.00 g, 5.12 mmol) in DMF (20 mL) was added acetic anhydride (1 mL) and triethylamine (1 mL) and the resulting solution was stirred for 4 h. The yellow precipitate was filtered, washed quickly with cold ethyl acetate, and dried in vacuo (1.139 g, 80%). 1H NMR (CDCl3): δ 9.20 (1H, d, J=2.5 Hz), 8.87 (1H, d, J=9.4 Hz), 8.55 (1H, dd, J=9.4, 2.5 Hz), 2.69 (3H, s), 2.63 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230020B2
Source datasetuspto-grants-2007_06
ORD IDord-3f0ccfe3275b4fee9ba9d415fcb41969
Source noteuspto-grants-2007_06