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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428313Generated: October 30, 2026

tert-Butyl methyl ether → HCID 86688194, compound

https://huagongshe.com/reaction/1428313

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methyl etherHCID 15413—
ReactantMaleic AcidHCID 444266—
ReactantNilotinibHCID 644241—
SolventEthanolHCID 702—
ProductHCID 86688194HCID 86688194—

Reaction Conditions

Temperature80 °C

Reaction Steps

Nilotinib base form A (4.00 g, 7.55 mmol) was stirred with EtOH abs (40 mL, 10V) and the suspension was heated to 80° C. Stirring was continued at the same temperature for 30 min. To the stirred suspension was added a solution of maleic acid (0.96 g, 8.31 mol. 1.1 eq) in EtOH abs (10 mL, 2.5V) in one portion. The resulting mixture was stirred at 80° C. for 1 h and then cooled to room temperature and stirred for another 6 h. The solids were isolated by filtration to give Nilotinib maleate form V. The obtained Nilotinib maleate form V was dried in a vacuum oven (35 mmHg) at 60° C. for 16 hours. The dried product was analyzed by PXRD and was found to be Nilotinib maleate form V. Mono maleate was obtained as confirmed by assay determination.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937082B2
Source datasetuspto-grants-2015_01
ORD IDord-a918427d839f429bb9fdf43bf615b9fe
Source noteuspto-grants-2015_01