Intermediate of API

143062-84-4

  • Product Name:(1R,2S)-FLUOROCYCLOPROPYLAMINE TOSYLATE
  • Molecular Formula:C7H8O3S.C3H6FN
  • Specifications:99%
  • Molecular Weight:247.29
Inquiry

Product Details;

CasNo: 143062-84-4

Molecular Formula: C7H8O3S.C3H6FN

High Purity (1R,2S)-FLUOROCYCLOPROPYLAMINE TOSYLATE 143062-84-4 Good Producer In Bulk Supply

  • Molecular Formula:C7H8O3S.C3H6FN
  • Molecular Weight:247.29
  • Boiling Point:418.2 °C at 760 mmHg 
  • Flash Point:206.7 °C 
  • PSA:88.77000 
  • LogP:3.07830 

143062-84-4 Relevant articles

Sitafloxacin three membered ring intermediate preparation method

-

Paragraph 0038-0064, (2017/07/07)

The invention discloses a preparation me...

Stereoselective synthesis of cis -2-fluorocyclopropanecarboxylic acid

Shibue, Taku,Fukuda, Yasumichi

, p. 7226 - 7231 (2014/08/18)

A rhodium-catalyzed cyclopropanation of ...

Synthesis of cis-2-fluorocyclopropylamine by stereoselective cyclopropanation under phase-transfer conditions

Matsuo, Jun-Ichi,Tani, Yu-Ichirou,Hayakawa, Yu-Ichirou

, p. 464 - 465 (2007/10/03)

cis-2-Fluorocyclopropylamine is stereose...

Synthetic studies on the key component of the new generation of quinolonecarboxylic acid, DU-6859. 1. Synthesis of (1R,2S)-2-fluorocyclopropylamine by the use of optical resolution

Tamura, Osamu,Hashimoto, Masaru,Kobayashi, Yuko,Katoh, Tadashi,Nakatani, Kazuhiko,Kamada, Masahiro,Hayakawa, Isao,Akiba, Toshifumi,Terashima, Shiro

, p. 3889 - 3904 (2007/10/02)

The title synthesis was achieved by empl...

143062-84-4 Process route

1,1,2-tribromo-2-fluoroethane
598-67-4

1,1,2-tribromo-2-fluoroethane

toluene-4-sulfonic acid
104-15-4

toluene-4-sulfonic acid

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

(1R,2S)-2-fluorocyclopropylamine p-toluenesulfonic acid salt
143062-84-4,185225-84-7

(1R,2S)-2-fluorocyclopropylamine p-toluenesulfonic acid salt

Conditions
Conditions Yield
1,1,2-tribromo-2-fluoroethane; malonic acid dimethyl ester; With potassium carbonate; In N,N-dimethyl-formamide; at 25 ℃; for 60h; Large scale;
With palladium on activated charcoal; hydrogen; In methanol; for 24h; under 3800.26 Torr; Autoclave; Large scale;
toluene-4-sulfonic acid; Temperature; Further stages; Large scale;
204 g
toluene-4-sulfonic acid
104-15-4

toluene-4-sulfonic acid

benzyl N-<(1R*,2S*)-2-fluorocyclopropyl>carbamate

benzyl N-<(1R*,2S*)-2-fluorocyclopropyl>carbamate

(1R*,2S*)-2-fluorocyclopropylammonium p-toluenesulfonate
143062-73-1,143062-84-4,151200-30-5,185225-84-7

(1R*,2S*)-2-fluorocyclopropylammonium p-toluenesulfonate

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; In methanol; for 1.5h; under 760 Torr; Ambient temperature;
87%

143062-84-4 Upstream products

  • 104-15-4
    104-15-4

    toluene-4-sulfonic acid

  • 142977-51-3
    142977-51-3

    (4R,5S)-3-((1R,2S)-2-Fluoro-cyclopropyl)-4,5-diphenyl-oxazolidin-2-one

  • 156481-81-1
    156481-81-1

    (R)-3-((1R,2S)-2-Fluoro-cyclopropyl)-4,5,5-triphenyl-oxazolidin-2-one

  • 127199-16-0
    127199-16-0

    tert-butyl N-<(1R,2S)-2-fluorocyclopropyl>carbamate

143062-84-4 Downstream products

  • 142977-49-9
    142977-49-9

    N-((1R,2S)-2-Fluoro-cyclopropyl)-3,5-dinitro-benzamide

Relevant Products