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Volumn 35, Issue 6, 2003, Pages 603-608

A reliable multigram synthesis of (±) doxazosin

Author keywords

[No Author keywords available]

Indexed keywords

DOXAZOSIN; MULTIGRAM SYNTHESIS;

EID: 0942300590     PISSN: 00304948     EISSN: 19455453     Source Type: Journal    
DOI: 10.1080/00304940309355360     Document Type: Article
Times cited : (7)

References (24)
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    • UK Patent 2, 007, 656B; CA
    • S. F. Campbell, UK Patent 2, 007, 656B; CA, 91: 74649u (1979).
    • (1979) , vol.91
    • Campbell, S.F.1
  • 12
    • 4644278011 scopus 로고    scopus 로고
    • US Patent 4, 188, 390; CA
    • S. F. Campbell, US Patent 4, 188, 390; CA, 91: 74649u (1999).
    • (1999) , vol.91
    • Campbell, S.F.1
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    • US Patent 3, 511, 836; CA
    • H-J. Hess, US Patent 3, 511, 836; CA, 71: 91519f (1969).
    • (1969) , vol.71
    • Hess, H.-J.1
  • 16
    • 85023862091 scopus 로고    scopus 로고
    • The purity of the product (±) (3) was determined by GC and found to be 98% (5% OV-17, 100-250°C, 10 °C /min)
    • The purity of the product (±) (3) was determined by GC and found to be 98% (5% OV-17, 100-250°C, 10 °C /min).
  • 17
    • 85023787148 scopus 로고    scopus 로고
    • The US and Indian patent applications are under review (CSIR Ref. No. NF/538/01)
    • The US and Indian patent applications are under review (CSIR Ref. No. NF/538/01).
  • 19
    • 85023808084 scopus 로고    scopus 로고
    • Polymorphic form of doxazosin mesylate (Form I), US Patents 6, 130, 218; CA, 129: 45312b (1998) and 6, 140, 334; CA, 129: 45310z (1998)
    • Polymorphic form of doxazosin mesylate (Form I), US Patents 6, 130, 218; CA, 129: 45312b (1998) and 6, 140, 334; CA, 129: 45310z (1998).
  • 20
    • 85023814442 scopus 로고    scopus 로고
    • The purity of the product (±) 4 was monitored by NMR and TLC. The NMR spectrum shows no trace of the hw-amide. We were unable to obtain a HPLC analysis of the product (±) 4 using YMC ODS 25cms, 5(1 column (50:50 mixture of acetonitrile and methanol modified with 0.05% v/v TEA in water)
    • The purity of the product (±) 4 was monitored by NMR and TLC. The NMR spectrum shows no trace of the hw-amide. We were unable to obtain a HPLC analysis of the product (±) 4 using YMC ODS 25cms, 5(1) column (50:50 mixture of acetonitrile and methanol modified with 0.05% v/v TEA in water).
  • 21
    • 85023860883 scopus 로고    scopus 로고
    • The US and Indian patent applications are under review (CSIR Ref. No. NF/428/02). European Patent No. 02021686.7
    • The US and Indian patent applications are under review (CSIR Ref. No. NF/428/02). European Patent No. 02021686.7
  • 22
    • 85023791479 scopus 로고    scopus 로고
    • Process optimization for the direct resolution of (±) 4 is in progress
    • Process optimization for the direct resolution of (±) 4 is in progress.
  • 23
    • 85023796129 scopus 로고    scopus 로고
    • The current ICH guideline for residual solvents in pharmaceutical active substances (ICH Guideline: Residual Solvents, Pharmeuropa, Vol. 8, No. 1, page 103, March 1996).
    • (1996) Residual Solvents, Pharmeuropa , vol.8 , Issue.1 , pp. 103
  • 24
    • 85023807242 scopus 로고    scopus 로고
    • A 100-kg batch production of this drug is currently under progress with Cadila Pharmaceuticals Ltd. Ahmedabad-380 009, Gujarat, India
    • A 100-kg batch production of this drug is currently under progress with Cadila Pharmaceuticals Ltd. Ahmedabad-380 009, Gujarat, India.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.