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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871664Generated: October 26, 2026

HCID 66876494, compound → 1-(3-tert-butyl-1-m-tolyl-1H-pyrazol-5-yl)-3-(3-(6-methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)phenyl)urea

https://huagongshe.com/reaction/871664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66876494HCID 66876494—
Reactant3-(6-Methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)anilineHCID 66876764—
Product1-(3-tert-butyl-1-m-tolyl-1H-pyrazol-5-yl)-3-(3-(6-methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)phenyl)ureaHCID 4424326388.9%

Reaction Steps

The title compound was prepared from 3-(6-methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)aniline (94 mg, 0.27 mmol) and phenyl 3-tert-butyl-1-m-tolyl-1H-pyrazol-5-ylcarbamate (115 mg, 0.33 mmol) using the procedure in Example 115C to give the title compound (145 mg, 0.24 mmol, 88%). 1H NMR (300 MHz, DMSO-d6) δ 9.25 (s, 1H), 8.67 (s, 1H), 8.45 (s, 1H), 7.81 (s, 1H), 7.48-7.21 (m, 9H), 6.37 (s, 1H), 4.32 (t, 2H), 3.99 (s, 3H), 3.76 (t, 2H), 3.36 (s, 3H), 2.38 (s, 3H), 1.27 (s, 9H); LC-MS (ESI) m/z 613 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969587B2
Source datasetuspto-grants-2015_03
ORD IDord-90de06b246a147628c63e3af3ff22af1
Source noteuspto-grants-2015_03