137234-71-0

  • Product Name:(2R,3S)-2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol L(-)-camphorsulfonate
  • Molecular Formula:C16H14F3N5O
  • Purity:99%
  • Molecular Weight:581.616
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Product Details;

CasNo: 137234-71-0

Molecular Formula: C16H14F3N5O

Buy High Quality High Purity (2R,3S)-2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol L(-)-camphorsulfonate 137234-71-0 Competitive Price

  • Molecular Formula:C10H16O4S*C16H14F3N5O
  • Molecular Weight:581.616
  • Vapor Pressure:3.63E-11mmHg at 25°C 
  • Melting Point:127-130℃ 
  • Refractive Index:1.616 
  • Boiling Point:508.6°C at 760 mmHg 
  • Flash Point:261.4°C 
  • PSA:156.54000 
  • Density:1.42g/cm3 
  • LogP:4.52730 

Voriconazole(Cas 137234-71-0) Usage

InChI:InChI=1/C16H14F3N5O/c1-10(15-14(19)5-20-7-22-15)16(25,6-24-9-21-8-23-24)12-3-2-11(17)4-13(12)18/h2-5,7-10,25H,6H2,1H3

137234-71-0 Relevant articles

Voriconazole synthesis method

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Paragraph 0011; 0048; 0064-0075, (2020/08/02)

The invention relates to a voriconazole ...

PROCESS FOR THE PREPARATION OF VORICONAZOLE

-

Page/Page column 10, (2012/01/13)

The present invention provides a process...

PROCESS FOR PREPARING VORICONAZOLE BY USING NEW INTERMEDIATES

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Page/Page column 14, (2011/09/14)

Provided is a process for preparing Vori...

PROCESS FOR THE PREPARATION OF VORICONAZOLE

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Page/Page column 5, (2010/04/23)

The present invention relates to an impr...

137234-71-0 Process route

(R)-10-camphorsulfonic acid
35963-20-3,61380-66-3

(R)-10-camphorsulfonic acid

2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butane-2-ol
137234-63-0,173967-54-9,188416-29-7

2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butane-2-ol

(2R,3S)-2-(2,4-difluorophenyl)-3-(5-fluoro-4-pyrimidinyl)-1-(1H-1,2,4-triazol-1-yl)-2-butanol (1R)-10-camphorsulfonate
188416-34-4,137234-71-0

(2R,3S)-2-(2,4-difluorophenyl)-3-(5-fluoro-4-pyrimidinyl)-1-(1H-1,2,4-triazol-1-yl)-2-butanol (1R)-10-camphorsulfonate

Conditions
Conditions Yield
In methanol; at 21 - 50 ℃; for 2.25h; Product distribution / selectivity;
59.11%
In methanol; ethyl acetate; Product distribution / selectivity; Heating / reflux;
97.15 % ee
In methanol; at 22 - 55 ℃; for 2h;
In methanol; ethyl acetate; at 20 - 23 ℃; Product distribution / selectivity; Heating / reflux;
99.41 % ee
In methanol; at 23 - 25 ℃; for 2h; Product distribution / selectivity; Heating / reflux;
93.87 % ee
In methanol; acetone; at -20 - 25 ℃; for 15h;
In methanol; acetone; Reflux;
12.3 g
(R)-10-camphorsulfonic acid
35963-20-3,61380-66-3

(R)-10-camphorsulfonic acid

2-(2,4-Difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol
182230-43-9,137234-63-0,173967-54-9,188416-29-7

2-(2,4-Difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol

(2R,3S)-2-(2,4-difluorophenyl)-3-(5-fluoro-4-pyrimidinyl)-1-(1H-1,2,4-triazol-1-yl)-2-butanol (1R)-10-camphorsulfonate
188416-34-4,137234-71-0

(2R,3S)-2-(2,4-difluorophenyl)-3-(5-fluoro-4-pyrimidinyl)-1-(1H-1,2,4-triazol-1-yl)-2-butanol (1R)-10-camphorsulfonate

Conditions
Conditions Yield
In methanol; at 0 - 2 ℃; Product distribution / selectivity;
81.52%
In acetone; at 45 - 55 ℃; for 2h; Large scale;
70%
In methanol; acetone; for 1h; Reflux;
40%

137234-71-0 Upstream products

  • 35963-20-3
    35963-20-3

    (R)-10-camphorsulfonic acid

  • 137234-63-0
    137234-63-0

    2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butane-2-ol

  • 137234-62-9
    137234-62-9

    voriconazole

  • 182230-43-9
    182230-43-9

    2-(2,4-Difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol

137234-71-0 Downstream products

  • 137234-62-9
    137234-62-9

    voriconazole

  • 35963-20-3
    35963-20-3

    (R)-10-camphorsulfonic acid

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