Carbamate → HCID 178465603, compound

HRID 427175Notes

Reaction equation

HRID 427175 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-203347c5864443fbb49deaf1ed010b82
Source dataset
uspto-grants-2001_11
Patent number
USRE037438E1

Reaction notes

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