Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetomilast | HCID 3025803 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86645102 | HCID 86645102 | 183.6% |
Reaction Steps
5 g of the anhydrous tetomilast type A crystal obtained in Example 1 (6) was dissolved in 400 ml of acetonitrile, while stirring under heating to reflux. The obtained solution was cooled to approximately 30° C. over about 1 hour, and it was then further cooled at 10° C. or lower for 1 hour, so as to obtain the precipitated crystal by filtration. The above precipitated crystal was dried at 50° C. for 3 hours, so as to obtain 5.1 g of a tetomilast acetonitrile solvate crystal in the form of a while platy crystal (yield: quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145404B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-5b5d84b32b3f48749e741a5d222e987d |
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| Source note | uspto-grants-2015_09 |
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