Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 89612672 | HCID 89612672 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 72725461 | HCID 72725461 | — |
Reaction Steps
In a flask was placed ethyl 2-(4-(6-fluoroindolin-1-yl)piperidine-1-carboxamido)thiazole-4-carboxylate (83.6 mg, 0.2 mmol) and EtOH (2 mL) was added. Then, 40 wt % CH3NH2(aq) (10 mL) was added and the resulting mixture was heated to 38-40° C. for 4 h. The resulting mixture was concentrated to remove EtOH and then partitioned in CH2Cl2/H2O (30 mL/30 mL). The aqueous layer was extracted with CH2Cl2 (30 mL). The combined organic layer was dried (Na2SO4) and filtered. The solvent was removed by roto-evaporator and the resulting residue re-solidified from CH2Cl2/hexane to yield 2-(4-(6-fluoroindolin-1-yl)piperidine-1-carboxamido)-N-methylthiazole-4-carboxamide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238658B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-f1131c6d492d43d589ca7f02aba48393 |
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| Source note | uspto-grants-2016_01 |
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