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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918014Generated: October 30, 2026

Phenyl 3-tert-butylisoxazol-5-ylcarbamate → 1-(3-(6,7-Bis(2-methoxyethoxy)quinazolin-4-ylthio)phenyl)-3-(3-tert-butylisoxazol-5-yl)urea

https://huagongshe.com/reaction/1918014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl 3-tert-butylisoxazol-5-ylcarbamateHCID 59394466—
Reactant3-(6,7-Bis(2-methoxyethoxy)quinazolin-4-ylthio)anilineHCID 66876874—
Product1-(3-(6,7-Bis(2-methoxyethoxy)quinazolin-4-ylthio)phenyl)-3-(3-tert-butylisoxazol-5-yl)ureaHCID 5826777152%

Reaction Steps

The title compound was prepared as described in Example 113C by using compound 3-(6,7-bis(2-methoxyethoxy)quinazolin-4-ylthio)aniline (138 mg, 0.34 mmol) and phenyl 3-tert-butylisoxazol-5-ylcarbamate described in Example 132A (116 mg, 0.45 mmol) to give 1-(3-(6,7-bis(2-methoxyethoxy)quinazolin-4-ylthio)phenyl)-3-(3-tert-butylisoxazol-5-yl)urea (100 mg, 52%) as a solid. 1H NMR (300 MHz, DMSO-d6) δ 10.20 (s, 1H), 9.05 (s, 1H), 8.69 (s, 1H), 7.85 (s, 1H), 7.46 (d, 1H), 7.45-7.38 (m, 3H), 7.31 (d, 1H), 6.05 (s, 1H), 4.36-4.32 (m, 4H), 3.79-3.76 (m, 4H), 3.37 (s, 6H), 1.24 (s, 9H); LC-MS (ESI) m/z 568 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-be24928ba13346efb80f5ad6ea810d57
Source noteuspto-grants-2013_12