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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099385Generated: October 31, 2026

7-{[1-(Tert-butoxycarbonyl)-piperidin-4-yl]oxy}-4-chloro-6-methoxyquinazoline → HCID 68903049, compound

https://huagongshe.com/reaction/2099385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-{[1-(Tert-butoxycarbonyl)-piperidin-4-yl]oxy}-4-chloro-6-methoxyquinazolineHCID 59682906—
ReactantTert-butyl (3-bromo-2-fluorophenyl)carbamateHCID 66729642—
ReactantHCID 68904833HCID 68904833—
ProductHCID 68903049HCID 68903049—

Reaction Steps

tert-Butyl 4-[(4-chloro-6-methoxyquinazolin-7-yl)oxy]piperidine-1-carboxylate was coupled with tert-butyl (3-bromo-2-fluorophenyl)carbamate using an analogous process to that described in Example 22 (preparation of starting materials) for the preparation of N-(3-chloro-4-fluorophenyl)-6-methoxy-7-(piperidin-4-yloxy)quinazolin-4-amine hydrochloride, to give N-(3-bromo-2-fluorophenyl)-6-methoxy-7-(piperidin-4-yloxy)quinazolin-4-amine hydrochloride; 1H NMR Spectrum: (DMSO d6) 1.85-2.1 (m, 2H), 2.1-2.32 (m, 2H), 3.0-3.35 (m, 4H), 4.02 (s, 3H), 4.83-5.0 (m, 1H), 7.3 (dd, 1H), 7.5-7.65 (m, 2H), 7.75 (dd, 1H), 8.45 (s, 1H), 8.8(s, 1H), 9.15 (bs, 2H), 11.86 (s, 1H); Mass Spectrum: (M+H)+ 447.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569577B2
Source datasetuspto-grants-2009_08
ORD IDord-a3b0b835cf6a453a9cd65a140dd6e908
Source noteuspto-grants-2009_08