Carbamate → HCID 178465603, compound

HRID 361727Notes

Reaction equation

HRID 361727 reaction equation
[C:1](=O)([O-])[NH2:2].F[C:6](F)(F)C(O)=O.Cl.C([NH:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][NH2:27])(OC(C)(C)C)=O>O1CCOCC1.CCOCC>[NH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][NH:27][C:1](=[NH:2])[CH3:6]

Participants

7

Procedure

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%).

Workup

  1. customthe solids were isolated by filtration

Sources & evidence

ORD record
ord-b410650da1804f88b424511226e5a711
Source dataset
uspto-grants-1999_02
Patent number
US05866612

Reaction notes

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