Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-amino-3,4-dihydroquinolin-2(1H)-one | HCID 4912759 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13505951 | HCID 13505951 | — |
Reaction Steps
To a solution of 6-amino-3,4-dihydrocarbostyril (3.24 g) in dimethylformamide (10 ml) is added 20N aqueous sodium hydroxide (1.2 ml) with stirring at room temperature. To the mixture is further added carbon disulfide (1.57 ml), and the mixture is stirred at the same temperature for 1 hour. To the reaction mixture is added methyl iodide (1.56 ml) under ice-cooling, and the mixture is stirred at the same temperature for 2.5 hours. After the reaction, the reaction mixture is poured into water, and the resulting precipitate is separated by filtration, washed with water, purified by silica gel column chromatography (solvent; chloroform:methanol=100:1), and recrystallized from methanol twice to give methyl (3,4-dihydrocarbostyril-6-yl)-dithiocarbamate (2.0 g) as yellow needles, m.p. 203.5°-205.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04593035 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-4622f196080149549d3a333f56f52abc |
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| Source note | uspto-grants-1986_06 |
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