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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30985Generated: October 28, 2026

Phosphorus oxychloride → Ethyl (7-methoxy-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl)acetate

https://huagongshe.com/reaction/30985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-(4-Methoxy-2-sulfamoyl-phenyl)-malonamic acid ethyl esterHCID 69309267—
ProductEthyl (7-methoxy-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl)acetateHCID 4694151679%

Reaction Steps

A mixture of 10 (8.0 g, 28 mmol) in phosphorous oxychloride (150 mL, 1.64 mol) was heated to reflux for 2.5 hours, then cooled to room temperature and concentrated in vacuo. The residue was then dissolved in ethyl acetate and neutralized with saturated aqueous sodium bicarbonate. The organic phase was washed with 2 N hydrochloric acid and then brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The solid product was then triturated in diethyl ether to produce 6.6 g of the desired product (4a) as a brown solid in 79% yield. See procedure described in International Patent Application No. PCT/US03/16374. 1H NMR (400 MHz, DMSO-d6): δ12.20 (s, 1H), 7.27 (m, 2 H), 7.20 (s, 1H), 4.14 (q, 2H, J=7.2 Hz), 3.73 (s, 3H), 3.66 (s, 2H), 1.21 (t, 3H, J=7.6 Hz); LC-MS (ESI+): m/e=299.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425552B2
Source datasetuspto-grants-2008_09
ORD IDord-c22644c799334538a84b730db18ddb84
Source noteuspto-grants-2008_09