Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | HCID 11216309 | HCID 11216309 | — |
| Product | HCID 9986150 | HCID 9986150 | 71% |
Reaction Steps
To N-(2-{5-tert-butyl-3-[(6-chloro-pyridine-3-carbonyl)-methanesulfonyl-amino]-2-methoxy-phenylcarbamoyl}-benzo[b]thiophen-7-yl)-6-chloro-nicotinamide (see Example 1) (33 mg) in a sealed tube was added 200 μL of cyclopropylamine. The reaction was purged with Ar and heated to 100° C. in the sealed tube 12 h. The reaction mixture was cooled to room temperature and diluted with EtOAc, washed by NH4Cl solution, water, and brine. The organics were dried over MgSO4, filtered, concentrated down to give a residue which was purified by flash chromatography on silica gel (CH2Cl2-2% MeOH/CH2Cl2) to provide the title compound (21 mg, 71%), m.p. >264° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550461B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-e2391624c0fb4e9298b48989133fbb78 |
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| Source note | uspto-grants-2009_06 |
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