Share a compound : Ethyl 3-amino-3-thioxopropanoate

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, Ethyl 3-amino-3-thioxopropanoate, other downstream synthetic routes, hurry up and to see.

Synthetic Route of 13621-50-6, The chemical industry reduces the impact on the environment during synthesis 13621-50-6, name is Ethyl 3-amino-3-thioxopropanoate, I believe this compound will play a more active role in future production and life.

Ethyl 2-amino-4-isopropyl-6-thio-5-cyano-1,4-dihydropyridine-3-carboxylate (IV). 1.0 g (10 mmol)of cyanothioacetamide II and a solution of sodiumethylate prepared from 0.23 g (10 mmol) of sodiumand 15 mL of anhydrous ethanol were added to a solution of 0.91 mL (10 mmol) of isobutyral Ia in15 mL of anhydrous ethanol at 20C. The reactionmixture was stirred during 5 min, then 1.5 g (10 mmol)of CH-acid III was added, and the mixture was stirredduring 30 min and incubated during 48 h. Next, themixture was diluted with 10% hydrochloric acid to pH5 upon stirring and incubated at room temperatureduring 48 h. The formed precipitate was filtered offand washed sequentially with water, ethanol, andhexane (Tables 1 and 2). Mass spectrum, m/z (Irel, %):266 (100) [M – 1]+.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, Ethyl 3-amino-3-thioxopropanoate, other downstream synthetic routes, hurry up and to see.

Reference:
Article; Dyachenko; Karpov; Dyachenko; Russian Journal of General Chemistry; vol. 85; 5; (2015); p. 1063 – 1068; Russian Journal of General Chemistry; vol. 85; 5; (2015); p. 1063 – 1068,6;,
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Extracurricular laboratory: Synthetic route of Ethyl 3-amino-3-thioxopropanoate

The chemical industry reduces the impact on the environment during synthesis Ethyl 3-amino-3-thioxopropanoate. I believe this compound will play a more active role in future production and life.

Related Products of 13621-50-6, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 13621-50-6, name is Ethyl 3-amino-3-thioxopropanoate, This compound has unique chemical properties. The synthetic route is as follows.

(step 6) A solution of the compound (107 mg, 0.30 mmol) obtained in step 5 and methyl 3-amino-3-thioxopropanoate (48.7 mg, 0.37 mmol) in EtOH (3 mL) was stirred at 90C for 14 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by NH-silica gel column chromatography (solvent gradient; 5?80% ethyl acetate/hexane) to give a crude product ethyl 2-(4-(1-tert-butyl-5-(4-methoxyphenyl)-1H-pyrazol-4-yl)thiazol-2-yl)acetate as a colorless oil, which was used for the next step without purification. MS (API) :400(M+H)

The chemical industry reduces the impact on the environment during synthesis Ethyl 3-amino-3-thioxopropanoate. I believe this compound will play a more active role in future production and life.

Reference:
Patent; Takeda Pharmaceutical Company Limited; YAMAMOTO, Satoshi; SHIRAI, Junya; OCHIDA, Atsuko; FUKASE, Yoshiyuki; TOMATA, Yoshihide; SATO, Ayumu; MIURA, Shotaro; YONEMORI, Kazuko; KOYAMA, Ryokichi; EP2738170; (2014); A1;,
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

The important role of 13621-50-6

The chemical industry reduces the impact on the environment during synthesis Ethyl 3-amino-3-thioxopropanoate. I believe this compound will play a more active role in future production and life.

Related Products of 13621-50-6, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 13621-50-6, name is Ethyl 3-amino-3-thioxopropanoate, This compound has unique chemical properties. The synthetic route is as follows.

A solution of 4-chlorophenacyl bromide (0.79 g, 3.38 mmol) and ethyl-3- amino-3-thioxopropanoate (0.50 g, 3.38 mmol) in EtOH (10 mL) was heated to 75C for 2 h under an atmosphere of N2. At the completion of the reaction the EtOH was evaporated, water was added and the mixture was washed with EtOAc (3 x 50 mL). The combined organic phases were washed with water and brine, dried over a2S04, filtered and concentrated. The crude residue was purified by silica chromatography (5% EtOAc/hexane) to afford ethyl 2-(4-(4-chlorophenyl)thiazol-2-yl)acetate (0.67 g, 70%).

The chemical industry reduces the impact on the environment during synthesis Ethyl 3-amino-3-thioxopropanoate. I believe this compound will play a more active role in future production and life.

Reference:
Patent; BIOTA SCIENTIFIC MANAGEMENT PTY LTD; HAYDON, David, John; CZAPLEWSKI, Lloyd, George; STOKES, Neil, Robert; DAVIES, David; COLLINS, Ian; PALMER, James, T; MITCHELL, Jeffrey, Peter; PITT, Gary Robert William; OFFERMANN, Daniel; WO2012/142671; (2012); A1;,
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics