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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918033Generated: November 1, 2026

Cesium carbonate → 3-(6-Ethoxy-7-methoxyquinazolin-4-ylthio)aniline

https://huagongshe.com/reaction/1918033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3-AminothiophenolHCID 31577—
Reactant4-Chloro-6-ethoxy-7-methoxyquinazolineHCID 10922620—
SolventTetrahydrofuranHCID 8028—
Product3-(6-Ethoxy-7-methoxyquinazolin-4-ylthio)anilineHCID 6687676246%

Reaction Steps

To a stirred suspension of cesium carbonate (3.60 g, 11.06 mmol) in THF (60 mL) was added 3-aminobenzenethiol (1.00 g, 7.99 mmol). After stirring for 30 minutes at rt, 4-chloro-6-ethoxy-7-methoxyquinazoline described in Example 11A (1.91 g, 7.99 mmol) was added and the reaction mixture was heated at rt for 15 h. The reaction mixture was cooled to rt and concentrated under reduced pressure to give a solid. Purification by silica gel column chromatography (eluting with 2% methanol in dichloromethane) afforded 3-(6-ethoxy-7-methoxyquinazolin-4-ylthio)aniline (1.20 g, 46%) as a cream solid, which did not require further purification. 1H NMR (400 MHz, DMSO-d6) δ 8.69 (s, 1H), 7.33 (s, 1H), 7.30 (s, 1H), 7.12 (dd, J=8, 8 Hz, 1H), 6.79 (s, 1H), 6.66-6.73 (m, 2H), 5.33 (brs, 2H), 4.21 (q, J=7 Hz, 2H), 3.98 (s, 3H), 1.43 (t, J=7 Hz, 3H); LC-MS (ESI) m/z 328 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-bb4c0c9da0fc45ac97a0defa7db890f3
Source noteuspto-grants-2013_12