Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 12888901 | HCID 12888901 | — |
| Reactant | N~1~-(2-Chloroethyl)-N'~1~-methyl-2-nitroethene-1,1-diamine | HCID 71421354 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ranisen | HCID 5039 | 45.7% |
Reaction Steps
To a stirred mixture of 5-[(dimethylamino)methyl]-2-furanmethane-thiol oxalate (1:1) (1.31 g) and N-(2-chloroethyl)-N'-methyl-2-nitro-1,1-ethenediamine (1.08 g) in water (20 ml) at 45° under an atmosphere of nitrogen was added a solution of potassium hydroxide (1.04 g) in water (3 ml). The solution was stirred at 45° for 2.5 hr. and at room temperature for 15 hr. The solution was then evaporated in vacuo, the residue dissolved in water and a stream of air passed into the mixture for 15 mins. The mixture was extracted with ether (2×15 ml) and the aqueous fraction evaporated in vacuo. To the residue was added tetrahydrofuran (70 ml), an excess of anhydrous sodium carbonate, and decolourising charcoal. After 1 hr the mixture was filtered, the filtrate evaporated in vacuo and the oily residue dissolved in 4-methyl-pentan-2-one (8 ml). The solid which separated was filtered and washed with 4-methylpentan-2-one to give the title compound (0.72 g), m.p. 63°-66°, which was not depressed on admixture with a sample prepared according to the method of Example 15 in British Patent No. 1,565,966.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04413135 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-1827064d4fce49bcb97adc22671873c9 |
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| Source note | uspto-grants-1983_11 |
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