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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444669Generated: October 31, 2026

2-Amino-4-[(methoxymethoxy)methyl]-3-thiophenesulfonamide → 1-[(Cyclopropylmethyl)amino]-4-hydroxy-3-{7-[(methoxymethoxy)methyl]-1,1-dioxido-4h-thieno[2,3-e][1,2,4]thiadiazin-3-yl}quinolin-2(1h)-one

https://huagongshe.com/reaction/1444669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-[(methoxymethoxy)methyl]-3-thiophenesulfonamideHCID 57455187—
Reactant3-[bis(methylthio)methylene]-1-[(cyclopropylmethyl)amino]quinoline-2,4(1H,3H)-dioneHCID 67063677—
Solvent1,4-DioxaneHCID 31275—
Product1-[(Cyclopropylmethyl)amino]-4-hydroxy-3-{7-[(methoxymethoxy)methyl]-1,1-dioxido-4h-thieno[2,3-e][1,2,4]thiadiazin-3-yl}quinolin-2(1h)-oneHCID 13597457952.3%

Reaction Steps

A solution of 3-[bis(methylthio)methylene]-1-[(cyclopropylmethyl)amino] quinoline -2,4(1H, 3H)-dione (500.3, 1.5 mmol) and the product of 2-amino-4-[(methoxy methoxy) methyl]thiophene-3-sulfonamide (377.62 mg, 1.5 mmol) in dioxane (15 mL) was stirred at reflux for 1.5 hours and concentrated under reduced pressure. The residue was purified by chromatography on silica gel eluting with 0% to 10% ethyl acetate/dichloromethane to give 1-[(cyclopropylmethyl)amino]-4-hydroxy-3-{7-[(methoxymethoxy)methyl]-1,1-dioxido-4H-thieno[2,3-e][1,2,4]thiadiazin-3-yl}quinolin -2(1H)-one (384.7 mg, 52%). 1H NMR (300 MHz, DMSO-d6) δ 0.15 (m, 2H) 0.42 (m, 2H) 1.01 (m, 1H) 2.84 (d, J=6.99 Hz, 2H) 4.64 (s, 2H) 4.71 (s, 2H) 6.36 (br s, 1H) 7.42 (m, 2H) 7.86 (m, 1H) 8.07 (d, J=8.46 Hz, 1H) 8.16 (m, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662958B2
Source datasetuspto-grants-2010_02
ORD IDord-8c823a1ad03e4db7b100de10b0b442f5
Source noteuspto-grants-2010_02