Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | HCID 178510043 | HCID 178510043 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178449571 | HCID 178449571 | — |
Reaction Steps
A mixture of 200 mg (0.521 mmol) of 3-(4-aminomethyl-phenylamino)-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine hydrate, 0.061 ml (0.548 mmol) of butyl isocyanate and 5 ml of THF is stirred at 20° C. for 15 hours and then concentrated by evaporation in vacuo. The residue is digested in 5 ml of boiling methanol, cooled to 5° C. and filtered, yielding 3-[4-(n-butylamino-carbonylamino-methyl)-phenylamino]-4-(3-chloro-phenyl-amino)-1H-pyrazolo[3,4-d]pyrimidine; m.p. 217-218° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251911B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-e2a0ff1e2d834bc18b324eab05b2ec29 |
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| Source note | uspto-grants-2001_06 |
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