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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30984Generated: October 25, 2026

P-Anisidine → 7-Methoxy-2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide

https://huagongshe.com/reaction/30984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventNitroethaneHCID 6587—
Product7-Methoxy-2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxideHCID 1252849095%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of chlorosulfonyl isocyanate (17 mL, 195 mmol.) was dissolved in 150 mL of nitroethane and cooled to −40° C. A solution of 4-methoxyaniline (Z) (20 g, 162 mmol) in 100 mL of nitroethane was then added drop-wise from a dropper funnel with stirring. After the addition was completed, the reaction was stirred for an additional 5 minutes and aluminum chloride (25 g, 195 mmol) was added. The mixture was then quickly heated to 110° C. with stirring for 20 minutes. The crude material was then poured onto ice and the precipitate was collected by suction filtration, washed with cold water, and dried in vacuo to produce 35 g of the desired product (8) as a purple powder in 95% yield. 1H NMR (400 MHz, DMSO-d6): δ 11.05 (s, 1H), 7.2 (m, 3H), 3.78 (s, 3H), 3.6 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425552B2
Source datasetuspto-grants-2008_09
ORD IDord-6983da0e423f4f0586daf65b5c99150f
Source noteuspto-grants-2008_09