Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | (4-chloro-3-trifluoromethyl-phenyl)-[5-(2-methylsulfonylpyrimidin-4-yloxy)-1H-benzimidazol-2-yl]-amine | HCID 178504847 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178482374 | HCID 178482374 | — |
Reaction Steps
To a solution of (4-chloro-3-trifluoromethyl-phenyl)-[5-(2-methanesulfonyl-pyrimidin-4-yloxy)-1H-benzimidazol-2-yl]-amine (Step B, 120 mg, 0.2 mmol, 1.0 eq.) in anhydrous THF (4 mL) was added 1 mL of 2 M CH3NH2 in THF (2 mmol, 10 eq). The solution was heated to 80° C. for 1 h. The THF was removed under reduced pressure and the crude was purified by column chromatography (0-10% MeOH/CH2Cl2 with 1% NH4OH) to yield pure (4-chloro-3-trifluoromethyl-phenyl)-[5-(2-methylamino-pyrimidin-4-yloxy)-1H-benzimidazol-2-yl]-amine. MS m/z=435.1 (M+H)+; MW Calc'd for C19H14ClF3N6O: 434.09.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531553B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-0bcea19a27624dedbc966d5062332b5b |
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| Source note | uspto-grants-2009_05 |
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