Method for synthesizing bendamustine hydrochloride intermediate
A technology of bendamustine hydrochloride and a synthesis method, which is applied in the field of chemical synthesis, can solve the problems of low selectivity of reduction, a large amount of sodium sulfide waste water, environmental pollution and the like, and achieves the advantages of shortening production cycle, short route and reducing cost. Effect
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2018-08-03
- Estimated Expiration
- Not applicable · inactive patent
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Abstract
Description
technical field
[0001] The invention relates to a synthesis method of a bendamustine hydrochloride intermediate, belonging to the technical field of chemical synthesis. Background technique
[0002] 1-Methyl-5-nitro-1H-benzimidazole-2-butyric acid ethyl ester is an important intermediate of bendamustine hydrochloride. Bendamustine hydrochloride is a bifunctional alkylating agent with antitumor effects. In 2003, it was launched in Germany under the trade name Ribomustine for the treatment of breast cancer and chronic lymphocytic leukemia. The trade name of bendamustine hydrochloride listed in the United States was Treanda, which was applied for by Cephalon and passed the priority approval process. Received FDA approval. In March 2008, the FDA first approved bendamustine hydrochloride for the treatment of chronic lymphocytic leukemia (CLL). In October of the same year, the FDA approved the second indication of the drug, that is, during the treatment of rituximab (rituximab,...
Examples
Embodiment 1
[0018] Take 51.6g of 2-chloro-5-nitroaniline into a three-neck flask, add 500ml of toluene, add 36g of glutaric anhydride at room temperature, heat to 80°C for 3 hours, cool to room temperature, filter, and filter cake at 70°C After drying, 145 g of a yellow solid intermediate was obtained, with a yield of 95%.
[0019] Add intermediate 1 obtained above into 150ml of 40% methylamine aqueous solution, heat to 50°C for 3 hours, cool to room temperature, adjust pH to 4-5 with 2N hydrochloric acid, precipitate a yellow solid, stir for 1 hour, filter, filter The cake was rinsed with toluene and dried at 70°C to obtain 40.5 g of yellow solid intermediate 2 with a yield of 91.7%.
[0020] Put the intermediate 2 prepared above into a three-necked flask, add 365ml of absolute ethanol, add 12ml of 98% concentrated sulfuric acid dropwise under stirring, heat to 80°C and reflux for 3h after the dropwise addition, cool to 45-50°C, pour the reaction solution into In saturated aqueous potas...