摘要:
The present disclosure discloses a method for continuously synthesizing N-Boc-2,5-dihydropyrrole. The method includes the following steps: cis-1,4 dichloro-2 butene is dissolved in an organic solvent, to prepare solution A; urotropine is dissolved in an organic solvent, to prepare solution B; the solution A and solution B are fed into a first continuous reaction device; a product overflow system of the first continuous reaction device is transferred to a second continuous reaction device, and concentrated hydrochloric acid is fed into the same; a product overflow system of the second continuous reaction device is transferred to a third continuous reaction device, and potassium carbonate is fed into the same; a product overflow system of the third continuous reaction device is transferred to a fourth continuous reaction device, and Boc acid anhydride solution is fed into the same; and a product of the fourth continuous reaction device is subjected to continuous solid-liquid separation, concentration and distillation, to obtain N-Boc-2,5-dihydropyrrole. By using technical solution of the present disclosure, the route involving high-risk materials is avoided, and the production capacity and yield are improved in a continuous manner.
摘要:
Provided is a ketoreductase mutant and applications thereof. Compared with an amino acid sequence shown in SEQ ID NO: 1, the amino acid sequence of the ketoreductase mutant includes at least one of the following mutation sites: L198P, S96W/I/L/V, M194L or L1526, herein "/" means "or." The ketoreductase mutant provides high selectivity and high activity with respect to a substrate ketone, and the application of the mutant in a catalytic reduction reaction of a ketone substrate may increase the production efficiency of a chiral alcohol compound corresponding thereto.
摘要:
The disclosure provides a method for preparing nilotinib. The preparation method includes the following steps: performing an aminocarbonylation reaction on a compound A and 3-(4-methyl-1H-imidazole-1-yl)-5-(trifluoromethyl) aniline to obtain an amination product; and performing deprotection treatment of an R group on the amination product to obtain the nilotinib, wherein the compound A has a structure shown in formula I, and in formula I, an R group is selected from benzyl, -COCF 3 , -CHO or -CO 2 R', where an R' group is C 1 ∼C 10 alkyl, C 1 ∼C 3 alkoxy ethyl or C 7 ∼C 19 aralkyl. The preparation method is short in synthesis route and mild in reaction condition. Moreover, with adoption of a special raw material, the preparation method may improve a yield of the nilotinib and simultaneously reduce process cost.
摘要翻译:本公开提供了制备尼罗替尼的方法。 该制备方法包括以下步骤:对化合物A和3-(4-甲基-1H-咪唑-1-基)-5-(三氟甲基)苯胺进行氨基羰基化反应,得到胺化产物; 进行氨基化产物上R基的脱保护处理得到尼罗替尼,其中化合物A具有式I所示结构,式I中R基选自苄基,-COCF 3,-CHO或-CO 2 R ',其中R'基团为C1〜C10烷基,C1〜C3烷氧基乙基或C7〜C19芳烷基。 该制备方法合成路线短,反应条件温和。 而且,通过采用特殊的原料,该制备方法可以提高尼罗替尼的产量,同时降低加工成本。
摘要:
The present invention relates to a preparation method for a chiral intermediate for use in statins, acquired with chloroacetic acid and benzyl alcohol as starting materials via a series of reactions, namely etherification, condensation, substitution, and asymmetric reduction. The preparation method provided in the present invention has a novel route of synthesis, allows an intermediate compound to be introduced conveniently into the chiral center of a glycol via enzyme reduction, and not only is low in costs, but also is reliable in quality. The route of synthesis provided in the present invention uses raw materials of low costs, has an easy to operate process, and provides a final product of great purity and high yield.
摘要:
The invention discloses an ozonization continuous reaction device, comprising a raw material inlet, a raw material distributing device, one or plurality of single reaction tubes, a product outlet and an air vent. The first end of the raw material distributing device is communicated with the raw material inlet; the first end of one or plurality of single reaction tubes is communicated with the second end of the raw material distributing device; the product outlet is communicated with the second end of the single reaction tube; ozone is conveyed to the single reaction tube via the air vent. The ozonization continuous reaction device provided by the invention realizes the large-scale and continuous production of the ozonization reaction on the basis of guaranteeing security; as the single reaction tube is arranged, the ozone amount and the liquid raw material existing in the single reaction tube in unit time become fewer, the reaction security is greatly improved; in addition, the liquid raw material and the ozone are continuously fed into the reaction device, the exhaust gas and the products are continuously discharged from the reaction device, the accumulation of the ozone is prevented, the security is greatly guaranteed, and the production capacity also can be improved to a higher level.
摘要:
The present disclosure provides a transaminase mutant and a method for preparing a chiral amine compound. Herein, the transaminase mutant includes: (a) a protein having an amino acid sequence as shown in SEQ ID NO: 1; or (b) a protein having an amino acid sequence as shown in SEQ ID NO: 2 or SEQ ID NO: 3; or (c) a protein that undergoes an amino acid mutation in at least one of the following sites of the amino acid sequence in (b): Y89, L380, N86, Y85, T91, P83, K90, S417, S424, F301, G164, T452 and the like, and has a transaminase function; or (d) a protein having more than 80% of the homology with the amino acid sequence defined in any one of (a), (b) or (c) and having a transaminase function.
摘要:
A transaminase mutant and use hereof, the amino acid sequence of the transaminase mutant is an amino acid sequence in which the amino acid sequence as represented by SEQ ID NO: 1 is mutated, the mutated amino acid position being one or more selected from among F89, K193, P243, V234, I262, Q280, V379, R416, A417 and C418. The enzymatic activity and/or stability of the transaminase mutant is improved.