Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Pivalic acid | HCID 6417 | — |
| Reactant | 2H-Indol-2-one, 5,6-diamino-1,3-dihydro-3,3-dimethyl- | HCID 13589237 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178441430 | HCID 178441430 | — |
Reaction Steps
Analogously to Example 11, 0.286 g. 5,6-diamino-3,3-dimethylindolin-2-one and 0.18 g. pivalic acid are heated with 3 g. polyphosphoric acid in a pre-heated bath for 30 minutes at 200° C. A further 0.18 g. pivalic acid are then added thereto and further heated for 30 minutes at 200° C. This procedure is repeated three times so that, in all, 0.9 g. pivalic acid are used with a total reaction time of 2.5 hours. After cooling, the mixture is dissolved in about 9 ml. water and adjusted to about pH 7 to 8 with concentrated aqueous ammonia solution. The precipitate obtained is filtered off with suction and washed with water to give 0.28 g. of the title compound; m.p. >300° C. For further purification, it is dissolved in a little hot ethanol, the turbid solution is treated with charcoal, the hot clear filtrate is evaporated in a vacuum and the evaporation residue is triturated with diethyl ether. One mole of the title compound thus obtained contains 1 mole of water; m.p. >300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04730003 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-02bc26d9c40a47e786da39bbe89fe0fe |
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| Source note | uspto-grants-1988_03 |
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