Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238089Generated: October 25, 2026

Formaldehyde → Vandetanib

https://huagongshe.com/reaction/238089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactanttert-Butyl 4-(((4-((4-bromo-2-fluorophenyl)amino)-6-methoxyquinazolin-7-yl)oxy)methyl)piperidine-1-carboxylateHCID 11049999—
SolventFormic AcidHCID 284—
ProductVandetanibHCID 308136188.3%

Reaction Conditions

Temperature95 °C

Reaction Steps

37% Aqueous formaldehyde (3.5 ml, 42 mmol) was added to a solution of 4-(4-bromo-2-fluoroanilino)-7-(1-(tert-butoxycarbonyl)piperidin-4-ylmethoxy)-6-methoxyquinazoline (3.49 g, 6.22 mmol), (prepared as described for the starting material in Example 1), in formic acid (35 ml). After heating at 95° C. for 4 hours the volatiles were removed under vacuum. The residue was suspended in water and the mixture was adjusted to pH10.5 by slow addition of a solution of 2N sodium hydroxide. The suspension was extracted with ethyl acetate. The organic layer was washed with brine, dried MgSO4 and evaporated to give 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline (2.61 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642608B2
Source datasetuspto-grants-2014_02
ORD IDord-b64a3f845a024b3baf1b329aa1ac6b92
Source noteuspto-grants-2014_02