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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631581Generated: October 27, 2026

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

https://huagongshe.com/reaction/631581

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 numberUS09320739B2
Source datasetuspto-grants-2016_04
ORD IDord-6bbf9bbf617649b0a499049956a8e917
Source noteuspto-grants-2016_04