메뉴 건너뛰기




Volumn 50, Issue 6, 2000, Pages 544-549

Synthesis of methylamino-2-phenyl-2-butyl-3,4,5-trimethoxybenzoate, the main bioactive metabolite of trimebutine maleate

Author keywords

CAS 39133 31 8; Debridat ; Desmethyl trimebutine, synthesis; Trimebutine, metabolite

Indexed keywords

BENZOIC ACID DERIVATIVE; DRUG METABOLITE; METHYLAMINO 2 PHENYL 2 BUTYL 3,4,5 TRIMETHOXYBENZOATE; TRIMEBUTINE MALEATE; UNCLASSIFIED DRUG;

EID: 0033914751     PISSN: 00044172     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0031-1300246     Document Type: Article
Times cited : (4)

References (16)
  • 1
    • 0003601534 scopus 로고
    • Merck Co.,Rahway, New Jersey
    • [1] See trimebutine in Merck Index, 11th Ed., p. 1526. Merck Co.,Rahway, New Jersey (1989)
    • (1989) Merck Index, 11th Ed. , pp. 1526
  • 2
    • 0033869678 scopus 로고    scopus 로고
    • Pharmacokinetics and bioequivalence of two trimebutine formulations in healthy volunteers using desmethyl-trimebutine levels
    • in press
    • [2] Saivin, S., Lavit, M., Michel, F. et al., Pharmacokinetics and Bioequivalence of Two Trimebutine Formulations in Healthy Volunteers Using Desmethyl-trimebutine Levels. Arzneim.-Forsch./Drug Res., in press (2000).
    • (2000) Arzneim.-Forsch./drug Res.
    • Saivin, S.1    Lavit, M.2    Michel, F.3
  • 3
    • 0033943047 scopus 로고    scopus 로고
    • Determination of trimebutine and desmethyl-trimebutine in human plasma by HPLC
    • in press
    • [3] Lavit, M., Saivin, S., Boudra, H. et al., Determination of Trimebutine and Desmethyl-trimebutine in Human Plasma by HPLC. Arzeinm-Forsch./Drug Res., in press (2000)
    • (2000) Arzeinm-Forsch./Drug Res.
    • Lavit, M.1    Saivin, S.2    Boudra, H.3
  • 4
    • 0017308082 scopus 로고
    • Alkylation and Michael additions of glycine ethyl ester. Use in α-amino acid synthesis and as acyl carbanion equivalent
    • [4] Stork, G., Leong, A. Y. N., Touzin, A.-M., Alkylation and Michael Additions of Glycine Ethyl Ester. Use in α-amino Acid Synthesis and as Acyl Carbanion Equivalent. J. Org. Chem. 41, 3491 (1976)
    • (1976) J. Org. Chem. , vol.41 , pp. 3491
    • Stork, G.1    Leong, A.Y.N.2    Touzin, A.-M.3
  • 5
    • 33845555590 scopus 로고
    • A mild and efficient route to Schiff base derivatives of amino acids
    • [5] O'Donnell, M. J., Polt, R. L., A Mild and Efficient Route to Schiff Base Derivatives of Amino Acids. J. Org. Chem. 47, 2663 (1982)
    • (1982) J. Org. Chem. , vol.47 , pp. 2663
    • O'Donnell, M.J.1    Polt, R.L.2
  • 6
    • 0029038316 scopus 로고
    • Diastereoselective alkylation of sultam-derived amino acid aldimines, preparation of Ca-methylated amino acids
    • [6] Ayoub, M., Chassaing, G., Loffet, A., Diastereoselective Alkylation of Sultam-Derived Amino Acid Aldimines, Preparation of Ca-Methylated Amino Acids. Tetrahedron Lett. 36, 4069 (1995)
    • (1995) Tetrahedron Lett. , vol.36 , pp. 4069
    • Ayoub, M.1    Chassaing, G.2    Loffet, A.3
  • 7
    • 0000147109 scopus 로고
    • Reaction of Schiff base anions with α,ω-dihaloalkanes: Synthetic route to cyclic α-aminoacid derivatives
    • [7] Joucla, M., El Goumzili, M., Reaction of Schiff Base Anions with α,ω-dihaloalkanes: Synthetic Route to Cyclic α-Aminoacid Derivatives. Tetrahedron Lett. 27, 1681 (1986)
    • (1986) Tetrahedron Lett. , vol.27 , pp. 1681
    • Joucla, M.1    El Goumzili, M.2
  • 9
    • 0001106559 scopus 로고
    • The use of N-formylamino acids in peptide synthesis
    • [9] Sheehan, J. C., Yang, D. D. H., The Use of N-Formylamino Acids in Peptide Synthesis. J. Am. Chem. Soc. 80, 1154 (1957)
    • (1957) J. Am. Chem. Soc. , vol.80 , pp. 1154
    • Sheehan, J.C.1    Yang, D.D.H.2
  • 10
    • 5244287483 scopus 로고
    • Reduction of bile acids and amides with lithium aluminium hydride
    • [10] Wessely, F., Swoboda, W., Reduction of Bile Acids and Amides with Lithium Aluminium Hydride. Monatsh. 82, 437 (1951)
    • (1951) Monatsh. , vol.82 , pp. 437
    • Wessely, F.1    Swoboda, W.2
  • 11
    • 0008540495 scopus 로고
    • The reduction of p-hydroxyformanilide by lithium aluminium hydride to N-methyl-paminophenol
    • [11] Ehrlich, J., The Reduction of p-Hydroxyformanilide by Lithium Aluminium Hydride to N-Methyl-paminophenol. J. Am. Chem. Soc. 70, 2286 (1948)
    • (1948) J. Am. Chem. Soc. , vol.70 , pp. 2286
    • Ehrlich, J.1
  • 12
    • 33947332318 scopus 로고
    • Selective reductions. IX. Reaction of lithium aluminium hydride with selected organic compounds containing representative functional groups
    • [12] Brown, H. C., Weissman, P. M., Yoon, N. M., Selective Reductions. IX. Reaction of Lithium Aluminium Hydride with Selected Organic Compounds Containing Representative Functional Groups. J. Am. Chem. Soc. 88, 1458 (1966)
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 1458
    • Brown, H.C.1    Weissman, P.M.2    Yoon, N.M.3
  • 13
    • 33947332955 scopus 로고
    • Selective Reductions. X. Reaction of Lithium Aluminium Hydride with Selected Organic Compounds Containing Representative Functional Groups. Comparison of the Reducing Characteristics of Lithium Aluminium Hydride and its Derivatives
    • [13] Brown, H. C., Yoon, N. M., Selective Reductions. X. Reaction of Lithium Aluminium Hydride with Selected Organic Compounds Containing Representative Functional Groups. Comparison of the Reducing Characteristics of Lithium Aluminium Hydride and its Derivatives. J. Am. Chem. Soc. 88, 1464 (1966)
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 1464
    • Brown, H.C.1    Yoon, N.M.2
  • 14
    • 0001087252 scopus 로고
    • The reduction of amides to amines via nitriles by lithium aluminium hydride
    • [14] Newnan, M. S., Fugunga, T., The Reduction of Amides to Amines via Nitriles by Lithium Aluminium Hydride. J. Am. Chem. Soc. 82, 693 (1960)
    • (1960) J. Am. Chem. Soc. , vol.82 , pp. 693
    • Newnan, M.S.1    Fugunga, T.2
  • 15
    • 0001138143 scopus 로고
    • Formylation of amines with chloral and reduction of the N-formyl derivatives with lithium aluminium hydride
    • [15] Blicke, F. F., Lu, C. J., Formylation of Amines with Chloral and Reduction of the N-Formyl Derivatives with Lithium Aluminium Hydride. J. Am. Chem. Soc. 73, 3933 (1951)
    • (1951) J. Am. Chem. Soc. , vol.73 , pp. 3933
    • Blicke, F.F.1    Lu, C.J.2
  • 16
    • 0001183962 scopus 로고
    • The formyl group as a hydrogenolyzable protecting group for peptide syntheses
    • [16] Losse, G., Nadolski, D., The Formyl Group as a Hydrogenolyzable Protecting Group for Peptide Syntheses. J. Prakt. Chem. 24, 118 (1964)
    • (1964) J. Prakt. Chem. , vol.24 , pp. 118
    • Losse, G.1    Nadolski, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.