反応 #514357

ord-203347c5864443fbb49deaf1ed010b82

反応方程式

O=C(O)C(F)(F)F
trifluoroactic acid
Cl
hydrochloric acid
CC(C)(C)OC(=O)NCCCCCCN
N-Boc-1,6-diaminohexane
NC(=O)[O-]
carbamate
CC(=N)NCCCCCCN
N-(6-aminohexyl)acetamidine
収率 66.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他the solids were isolated by filtration

実験手順

To a 0° C. stirred solution of 1.0 g (4.62 mmol) of N-Boc-1,6-diaminohexane in 30 ml ethanol was added 0.86 g (4.62 mmol) of intermediate B. After two hours the solution was concentrated, diluted with water (50 ml), and extracted with ether twice. The aqueous phase was freeze-dried to yield 0.9 g of white sticky solid tert-butyl N-(6-((acetimidoyl) amino)hexyl)carbamate intermediate. A suspension of the carbamate above (0.88 g, 3 mmol) in 15 ml dioxane and 7.5 ml trifluoroactic acid was treated with 10 ml (40 mmol) of 4N hydrochloric acid in dioxane solution with stirring overnight. The mixture was diluted with ether (50 ml) and the solids were isolated by filtration to provide 0.7 g N-(6-aminohexyl)acetamidine as a white solid (66% yield from N-Boc-1,6-diaminohexane). M.P.=163°-164° C. Mass spectrum (CI) 158.1 (MH+, 100%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE037438E1uspto-grants-2001_11