Reaktion #2144489

ord-097e92c4452741b99e1b3e8083a84330

Reaktionsgleichung

CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](C#CCOS(C)(=O)=O)CC1
trans-Methanesulfonic acid 3-[4-(tert-butoxycarbonyl-methyl-amino)-cyclohexyl]-prop-2-ynyl ester
O=C(O)C(F)(F)F
TFA
→
CN[C@H]1CC[C@H](C#CCOS(C)(=O)=O)CC1
trans-Methanesulfonic acid 3-(4-methylamino-cyclohexyl)-prop-2-ynyl ester
Ausbeute 191.1%

Edukte

CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](C#CCOS(C)(=O)=O)CC1
trans-Methanesulfonic acid 3-[4-(tert-butoxycarbonyl-methyl-amino)-cyclohexyl]-prop-2-ynyl ester
O=C(O)C(F)(F)F
TFA

Reagenzien

Keine

Lösungsmittel

ClCCl
CH2Cl2

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe reaction was evaporated
  2. 2
    Sonstigeevaporated again with toluene (4 times)

Vorschrift

A solution of 6.02 g (17.43 mmol) of trans-Methanesulfonic acid 3-[4-(tert-butoxycarbonyl-methyl-amino)-cyclohexyl]-prop-2-ynyl ester in 95 ml CH2Cl2 was treated at 0° C. with 45 ml TFA (for 20 min). After 30 min at this temperature, the reaction was evaporated and evaporated again with toluene (4 times) to give 8.17 g (quantitative) of crude trans-Methanesulfonic acid 3-(4-methylamino-cyclohexyl)-prop-2-ynyl ester.trifluoroacetate, MS: 245 (M).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07335687B2uspto-grants-2008_02