Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | HCID 21101363 | HCID 21101363 | — |
| Product | HCID 10226138 | HCID 10226138 | — |
Reaction Steps
A mixture of N-[4-chloro-6-(1-piperidinyl)-2-pyrimidinyl]-N-ethyl-N-[2-(1H-indol-3-yl)ethyl]amine (33.4 mg, 0.087 mmol) and p-toluidine (47 mg, 0.43 mmol) was heated neat under argon at 160° C. in a sealed tube for 12 hours. The crude material was purified by preparative TLC, eluting with hexane/ethyl acetate (4:1). N2-Ethyl-N2-[2-(1H-3-indolyl) ethyl]-N4-(4-methylphenyl)-6-piperidino-2,4-pyrimidinediamine was obtained, from a band at Rf=0.37, as a solid (15 mg, 0.033 mmol, 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07220775B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-a94bf61c68564bc8b4831512b23b45da |
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| Source note | uspto-grants-2007_05 |
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