CAS: 13492-01-8; Trans-2-Phenylcyclopropanamine Hemisulfate

该化合物是一种化学化合物,主要被认为是用于治疗抑郁的单胺氧化酶抑制剂(MAOI),是苯乙胺的衍生物,其特点是能够抑制酶单胺氧化酶,造成脑中血清素,无肾麻素和多巴胺等...

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(1SR,2SR)-2-phenylcyclopropanecarbonyl chloride (E)-3-phenylacrylic acid trans-2-phenylcyclopropane-1-carboxylic acidmethyl 7-(4-((2-phenylcyclopropyl)carbamoyl)phenoxy)-6-cyano-3,4-dihydro-2H-chromene-4-carboxylate tert-butyl (trans-2-phenylcyclopropyl)carbamate 2-phenylcyclopropylamine N-methyl-trans-2-phenylcyclopropylamine hydr°Chloride

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    专利号:US-4016204-A
    优先权日:1975-10-31
    标 题 :Method of synthesis of trans-2-phenylcyclopropylamine
    发明人:RAJADHYAKSHA VITHAL JAGANNATH
    权利人:NELSON RES & DEV
    摘要:An improved method of synthesis of trans-2-phenylcyclopropylamine wherein the improvement comprises isomerizing an intermediate ester, namely, cis,trans-ethyl-2-phenylcyclopropanecarboxylate, by reacting said ester with anhydrous sodium ethoxide, to form a reaction product containing not more than about 5 percent cis ester and further reacting said resultant product to form trans-2-phenylcyclopropylamine.

    专利号:EP-3617181-A1
    优先权日:2018-08-30
    标题:Synthesis of trans-2-phenylcyclopropylamine or a salt or solvate thereof
    发明人:BREUNING ALEXANDER; LIMMERT MICHAEL; DELLING AXEL; HOFMEIER HARALD; HULTSCH JANA; MICKSCH MAIK; SOMMER CHRISTIAN
    权利人:AREVIPHARMA GMBH
    摘要:The present invention relates to the field of manufacturing trans-2-phenylcyclopropylamine or a salt or solvate thereof, in particular in the form of the sulphate salt. The obtained product, particularly when in the form of the synthesis of trans-2-phenylcyclopropylamine sulphate, is exceptionally pure, substantially free from reactants and reagents that are mutagenic, hazardous or of great concern to the health of humans or the environment.

    专利号:IE-44046-B1
    优先权日:1975-10-31
    标题 :Improved method of synthesis of trans-2-phenylcycloprpylamine

    专利号:GB-1561725-A
    优先权日:1975-10-31
    标题:Method of synthesis of trans-2-phenylcycloproylamine

    专利号:US-11459325-B2
    优先权日:2018-01-31
    标题:Heterocyclic compound
    发明人:TANAKA YUTA; OHASHI TOMOHIRO; IKEDA ZENICHI; TANAKA YUTA; PÜNNER FLORIAN; YAMAMOTO TAKESHI; KAKEGAWA KEIKO; KIKUCHI FUMIAKI; MORISHITA NAO; KASAHARA TAKAHITO; SETO MASAKI; NAKAMURA MINORU; TAKAMI KAZUAKI; MURAKAMI MASATAKA; DAINI MASAKI; MIKAMI SATOSHI; SASAKI MINORU
    权利人:TAKEDA PHARMACEUTICALS CO
    摘要:The present invention provides a compound having a glucosylceramide lowering action (e.g., promoting glucosylceramide metabolism, inhibition of glucosylceramide synthesis, promoting glucosylceramide catabolism, etc.), which is expected to be useful as an agent for the prophylaxis or treatment of lysosome diseases (e.g., Gaucher's disease), neurodegenerative diseases (e.g., Parkinson's disease, Lewy body dementia, multiple-system atrophy) and the like. n The present invention relates to a compound represented by the formula (I): n nwherein each symbol is as described in the specification, or a salt thereof.

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    主要参考文献


    1: Gahr M, Schönfeldt-Lecuona C, Kölle MA, Freudenmann RW. Intoxications with the monoamine oxidase inhibitor tranylcypromine: an analysis of fatal and non-fatal events. Eur Neuropsychopharmacol. 2013 Nov;23(11):1364-72. doi: 10.1016/j.euroneuro.2013.05.009. Epub 2013 Jun 19. Review. doi: 10.5414/CP201898. Review. doi: 10.1055/s-0032-1333265. Epub 2013 Jan 28. Review. Review. Review.
    6: Frieling H, Bleich S. Tranylcypromine: new perspectives on an "old" drug. Eur Arch Psychiatry Clin Neurosci. 2006 Aug;256(5):268-73. Review. Review. Review.

    合成参考文献


    摘要:Psychotropic Drugs and Related Compounds, 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972, -(359), 1972
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