Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Alaninol | HCID 80307 | — |
| Reactant | HCID 57974150 | HCID 57974150 | — |
| Product | HCID 57974178 | HCID 57974178 | 52% |
Reaction Steps
Ethyl 2-[(5-chloro-2-{[3-(4-methyl-1-piperazinyl)phenyl]amino}-4-pyrimidinyl)amino]benzoate (150 mg, 0.32 mmol) and (2S)-2-amino-1-propanol (0.5 mL) were combined in a vessel, which was sealed and heated with stirring at 95° C. for 18 h. The reaction was cooled to room temperature and the solid was filtered off and washed with ethanol/water (1:1 ratio) and ethyl ether to afford the product (82 mg, 52% yield) as a white solid. MS: M(C25H30ClN7O2)=496.01, (M+H)+=496.2 and 498.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884098B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-dcf05306819f4711a28e8e047dd0bdbf |
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| Source note | uspto-grants-2011_02 |
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