Réaction #1869178

ord-b14c93ecec2d476e8a8652d824d39716

Équation de réaction

CCCCN1C(=O)N(CC(C)C)C(=O)C12CCNCC2
compound
CCCCN1C(=O)N(CC(C)C)C(=O)C12CCNCC2
1-butyl-3-isobutyl-1,3,8-triazaspiro[4.5]decane-2,4-dione
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
O=S([O-])Cl
benzenesulfonylchloride resin
Cc1ccc(S(=O)(=O)Cl)cc1
TsCl
OCCCCCCc1ccccc1
6-phenylhexanol
CCCCN1C(=O)N(CC(C)C)C(=O)C12CCN(CCCCCCc1ccccc1)CC2.Cl
title compound
Rendement 58.9%
CCCCN1C(=O)N(CC(C)C)C(=O)C12CCN(CCCCCCc1ccccc1)CC2.Cl
1-butyl-3-isobutyl-8-(6-phenylhexyl)-1,3,8-triazaspiro[4.5]decane-2,4-dione hydrochloride
Rendement 58.9%

Solvants

Conditions de réaction

Température
70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Filtrationfiltrated
  2. 2
    LavageThe resin was washed with acetonitrile (3 mL, three times)
  3. 3
    LavageThe filtrate and rinsed solution
  4. 4
    Concentrationconcentrated
  5. 5
    AutreThe residue was purified by column chromatography on silica gel (chloroform:methanol=25:1)
  6. 6
    workup.ADDITIONadded 4N hydrochloric acid in ethyl acetate
  7. 7
    Concentrationconcentrated

Mode opératoire

To a solution of the compound prepared in Example 1 (28 mg) and N,N-diisopropylethylamine (155 mg) in acetonitrile (3 mL) were added benzenesulfonylchloride resin (Argonaut, product name PS-TsCl, product number 800276, 1.22 mmol/g, 0.20 mmol) (164 mg) and sulfonyl resin (175 mg) which is prepared from 6-phenylhexanol (345 mg). The mixture was stirred for 18 hours at 70° C. and then filtrated. The resin was washed with acetonitrile (3 mL, three times). The filtrate and rinsed solution were combined and concentrated. The residue was purified by column chromatography on silica gel (chloroform:methanol=25:1), added 4N hydrochloric acid in ethyl acetate and concentrated to give the title compound (28 mg) having the following physical data.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07498323B2uspto-grants-2009_03