Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 178510043 | HCID 178510043 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178514086 | HCID 178514086 | — |
Reaction Steps
A mixture of 150 mg (0.391 mmol) of 3-(4-aminomethyl-phenylamino)-4-(3chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine hydrate (see Step 77.5), 95 mg (1.17 mmol) of potassium cyanate, 3 ml of ethanol, 3 ml of water and 0.0258 ml (0.451 mmol) of acetic acid is heated under reflux for 1 hour. After cooling to about 20° C., filtration and recrystallization of the filtration residue from methanol/water, 4-(3-chloro-phenylamino)-3-(4-{ureido-methyl}-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine is obtained; m.p. >280° C.; FAB-MS: (M+H)+=409.
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-7fd16b0d29504e5cbd618fbaffe2b66c |
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| Source note | uspto-grants-2001_06 |
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