Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 53410282 | HCID 53410282 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 53261245 | HCID 53261245 | 91% |
Reaction Steps
100 mg of 6-chloro-N-(4-methoxyphenyl)pyrimidine-4-amine in the form of a hydrochloride, 57 mg of methylamine and 238 mg of DIPEA were dissolved in 1 mL of n-BuOH in a screw cap vial and the mixture obtained was heated to 120° C. for 1 hour. Progress of the reaction was monitored by TLC. Upon termination of the reaction n-BuOH. was evaporated off and the evaporation residue was subjected to crystallization from n-BuOH/EtOH solvent mixture. N4-(4-Methoxyphenyl)-N6-methylpyrimidine-4,6-diamine was obtained in the form of a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08986994B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-5c2799bf383e498db237b37a2699ca8f |
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| Source note | uspto-grants-2015_03 |
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