Acetone → HCID 86734724, compound
Reaction equation
[Na].S(O)(O)(=O)=[O:3].[NH:7]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][NH:17][C:18]([NH2:20])=[NH:19])[C:8]([NH2:10])=[NH:9].[Cl:21][C:22]1[CH:27]=[CH:26][C:25]([N:28]=[C:29]=[S:30])=[CH:24][CH:23]=1.C[OH:32].[CH3:33][C:34]([CH3:36])=[O:35]>C(O)(=O)C>[C:34]([OH:32])(=[O:35])[CH3:36].[C:34]([OH:3])(=[O:35])[CH3:36].[Cl:21][C:22]1[CH:27]=[CH:26][C:25]([NH:28][C:29]([N:7]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][N:17]([C:29](=[S:30])[NH:28][C:34]2[CH:36]=[CH:27][C:22]([Cl:21])=[CH:23][CH:33]=2)[C:18]([NH2:20])=[NH:19])[C:8]([NH2:10])=[NH:9])=[S:30])=[CH:24][CH:23]=1Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium (0.05g, 0.02m) is dissolved in dry acetone and 3.0 grams (0.01m) of 1,6-bis(guanidino)hexane sulfate is added. The resulting suspension is stirred for two hours at room temperature and thereafter 3.4 grams (0.02m) of 4-chlorophenyl isothiocyanate is added. The mixture is heated at 60° for 3 hours, then stirred overnight at room temperature. Ten milliliters of methanol are added to decompose residual sodium. The solvent is distilled and the residue is washed by decantation with several portions of water to leave the product as the free base. The residue is dissolved in 60ml. of warm acetic acid. The solution is cooled and the diacetate which precipitates is collected on a filter, washed with acetic acid, then recrystallized from acetic acid, M.P. 145°-148° C.
Workup
- temperatureThe mixture is heated at 60° for 3 hours
- stirringstirred overnight at room temperature
- distillationThe solvent is distilled
- washthe residue is washed by decantation with several portions of water
- customto leave the product as the free base
- dissolutionThe residue is dissolved in 60ml
- temperatureThe solution is cooled
- customthe diacetate which precipitates
- customis collected on a filter
- washwashed with acetic acid
- customrecrystallized from acetic acid, M.P. 145°-148° C.
Sources & evidence
- ORD record
- ord-3af15ceb4152405e89ee2c5600b4ed5d
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04115447
Reaction notes
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