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ChemicalBook CAS DataBase List 4-Ethyl-2,3-dioxo-1-piperazine carbonyl chloride

4-Ethyl-2,3-dioxo-1-piperazine carbonyl chloride synthesis

2synthesis methods
-

Yield:59703-00-3 94.3%

Reaction Conditions:

with pyridine;dmap;chloro-trimethyl-silane in dichloromethane at -25 - -20;

Steps:

1.1-3.1; 1.1 Example 1: (improved)
1) taking N-ethyldioxypiperazine 14.2 g (0.10 mol),Transfer to a 500 mL three-necked flask, stir, and add 200 mL of dichloromethane.Cool down to -25 to -20 ° C, add 16.3 g (0.15 mol) TMCS,Control temperature -25 ~ -20 ° C, add 11.9g (0.15mol) pyridine,Adding 0.018 g of DMAP, adding 11.9 g (0.04 mol) of triphosgene in batches at a temperature of -25 to -20 ° C, and maintaining the reaction for 30-60 minutes;After the reaction was completed, suction filtration, washing with 30 mL of dichloromethane and distillation to dryness under reduced pressure.Add 100 mL of n-hexane to crystallize and filter by suction.Drying gave 19.3 g of N-ethylbisoxypiperazine chloride in a yield of 94.3%.

References:

Qilu Tianhe Huishi (Leling) Pharmaceutical Co., Ltd.;Qilu Tianhe Huishi Pharmaceutical Co., Ltd.;Sun Zhengjun;Fan Changying;Sun Yue;Li Yong CN109734725, 2019, A Location in patent:Paragraph 0028-0029; 0031-0032; 0034-0035; 0037-0038; 0041

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