FR1160693A - Procédé de préparation de p-bis-(2-chloréthyl)-aminophénylalanine - Google Patents

Procédé de préparation de p-bis-(2-chloréthyl)-aminophénylalanine

Info

Publication number
FR1160693A
FR1160693A FR1160693DA FR1160693A FR 1160693 A FR1160693 A FR 1160693A FR 1160693D A FR1160693D A FR 1160693DA FR 1160693 A FR1160693 A FR 1160693A
Authority
FR
France
Prior art keywords
chlorethyl
aminophenylalanine
bis
preparing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
Other languages
English (en)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Research Development Corp UK
Original Assignee
National Research Development Corp UK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by National Research Development Corp UK filed Critical National Research Development Corp UK
Application granted granted Critical
Publication of FR1160693A publication Critical patent/FR1160693A/fr
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
FR1160693D 1953-03-17 1954-03-16 Procédé de préparation de p-bis-(2-chloréthyl)-aminophénylalanine Expired FR1160693A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB335688X 1953-03-17

Publications (1)

Publication Number Publication Date
FR1160693A true FR1160693A (fr) 1958-07-24

Family

ID=10354626

Family Applications (1)

Application Number Title Priority Date Filing Date
FR1160693D Expired FR1160693A (fr) 1953-03-17 1954-03-16 Procédé de préparation de p-bis-(2-chloréthyl)-aminophénylalanine

Country Status (5)

Country Link
US (1) US3032584A (fr)
CH (2) CH335688A (fr)
DE (1) DE965036C (fr)
FR (1) FR1160693A (fr)
GB (1) GB750155A (fr)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
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GB915751A (en) * 1960-04-04 1963-01-16 Nat Res Dev Substituted alanines
JPS62192357A (ja) * 1986-02-19 1987-08-22 Kureha Chem Ind Co Ltd Ｎ−フタロイル−ｐ−ニトロ−Ｌ−フエニルアラニンの製造方法
US4835182A (en) * 1987-08-21 1989-05-30 The United States Of America As Represented By The Department Of Health And Human Services Enhancing drug delivery to the brain
GB8727157D0 (en) * 1987-11-19 1987-12-23 Wellcome Found Pharmaceutical formulations
GB8820850D0 (en) * 1988-09-05 1988-10-05 Cancer Res Campaign Tech Improvements relating to pro-drugs
EA000885B1 (ru) * 1996-02-12 2000-06-26 Олег Ильич ЭПШТЕЙН Лекарственное средство и способ медикаментозного воздействия на организм
US20040072889A1 (en) * 1997-04-21 2004-04-15 Pharmacia Corporation Method of using a COX-2 inhibitor and an alkylating-type antineoplastic agent as a combination therapy in the treatment of neoplasia
EP1191948A2 (fr) * 1999-06-11 2002-04-03 Neorx Corporation Complexe a forte dose de radionucleides destine a la suppression de la moelle osseuse
US7094885B2 (en) 1999-07-11 2006-08-22 Neorx Corporation Skeletal-targeted radiation to treat bone-associated pathologies
SE0002202D0 (sv) 2000-06-13 2000-06-13 Karolinska Innovations Ab New peptides
US6992207B2 (en) * 2000-06-13 2006-01-31 Oncopeptides Ab Melphalan derivatives and their use as cancer chemotherapeutic drugs
RU2181297C2 (ru) * 2000-06-20 2002-04-20 Эпштейн Олег Ильич Способ лечения патологического синдрома и лекарственное средство
WO2002062398A2 (fr) 2001-01-08 2002-08-15 Neorx Corporation Composes, compositions et methodes therapeutiques et diagnostiques
US7829084B2 (en) 2001-01-17 2010-11-09 Trubion Pharmaceuticals, Inc. Binding constructs and methods for use thereof
UA76639C2 (uk) * 2002-08-02 2006-08-15 Олєг Ільіч Епштєйн Гомеопатичний лікарський засіб та спосіб лікування еректильних дисфункцій
RU2253478C1 (ru) * 2003-10-01 2005-06-10 Эпштейн Олег Ильич Средство для потенцирования лечебных эффектов - усиления действия лекарственного вещества
WO2007096647A2 (fr) * 2006-02-27 2007-08-30 Sterix Limited Composé
CN100491339C (zh) * 2007-04-20 2009-05-27 苏州市立德化学有限公司 一种抗肿瘤药物美法仑的合成工艺
US20110092595A1 (en) * 2008-02-15 2011-04-21 Garth Powis Compositions and Methods for Treating Lung Cancer
WO2009117164A1 (fr) * 2008-03-20 2009-09-24 Navinta Llc Procédé permettant de produire du melphalan optiquement pur
EP2191840A1 (fr) 2008-11-28 2010-06-02 Sanofi-Aventis Combinaisons antitumorales contenant des anticorps reconnaissant spécifiquement les CD38 et melphalan
WO2010105008A2 (fr) 2009-03-12 2010-09-16 Genentech, Inc. Combinaisons de composés inhibiteurs de phosphoinositide 3-kinase et d'agents chimiothérapeutiques pour le traitement de tumeurs malignes hématopoïétiques
US11020363B2 (en) 2009-05-29 2021-06-01 Cydex Pharmaceuticals, Inc. Injectable nitrogen mustard compositions comprising a cyclodextrin derivative and methods of making and using the same
CN102458114A (zh) * 2009-05-29 2012-05-16 锡德克斯药物公司 包含环糊精衍生物的可注射美法仑组合物及其制备和使用方法
CN102625807B (zh) 2009-09-08 2016-03-09 霍夫曼-拉罗奇有限公司 4-取代的吡啶-3-基-甲酰胺化合物和使用方法
AR077384A1 (es) 2010-07-05 2011-08-24 Eriochem Sa Una formulacion farmaceutica inyectable de melfalano.
US9308275B2 (en) 2010-07-15 2016-04-12 Oleg Iliich Epshtein Method of increasing the effect of an activated-potentiated form of an antibody
CN102030671B (zh) * 2010-10-26 2014-02-19 浙江凯普化工有限公司 医药级美法仑及其盐酸一盐、二盐的制备方法
US8921596B2 (en) 2010-11-04 2014-12-30 Emcure Pharmaceuticals, Ltd. Process for the preparation of melphalan hydrochloride
UA112170C2 (uk) 2010-12-10 2016-08-10 Санофі Протипухлинна комбінація, що містить антитіло, яке специфічно розпізнає cd38, і бортезоміб
PL3656393T3 (pl) 2011-04-28 2023-01-16 Oncopeptides Ab Liofilizowany preparat cytotoksycznych dipeptydów
CN102757357B (zh) * 2012-07-25 2014-04-23 平湖优康药物研发中心 一种抗肿瘤药物美法仑的合成工艺
US9963422B2 (en) 2013-03-11 2018-05-08 Biophore India Pharmaceuticals Pvt. Ltd. Process for the synthesis of melphalan and the hydrochloride salt
ITMI20130896A1 (it) 2013-05-31 2014-12-01 Farmabios Spa Processo di purificazione di melphalan
AU2015371308A1 (en) 2014-12-23 2017-08-03 Intellectual Property Associates, Llc Methods and formulations for transdermal administration
US20190083527A1 (en) 2017-09-15 2019-03-21 Ampersand Biopharmaceuticals, Inc. Method of administration and treatment
IT201900025348A1 (it) 2019-12-23 2021-06-23 Indena Spa Procedimento per la sintesi di melfalan
CN114315618A (zh) * 2021-12-04 2022-04-12 浙江恒腾福生物科技集团有限公司 一种合成美法仑的制备方法

Also Published As

Publication number Publication date
GB750155A (en) 1956-06-13
CH335688A (de) 1959-01-31
US3032584A (en) 1962-05-01
DE965036C (de) 1957-05-29
CH339216A (de) 1959-06-30

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