Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | HCID 86607570 | HCID 86607570 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 11530141 | HCID 11530141 | — |
Reaction Steps
The title compound was prepared from 3-tert-Butoxy-carbonylamino-6-methyl-pyridine-2-carboxylic acid methyl ester in accordance with the general method of example 4; step 2 using 2-amino-5-fluoro-6-methylpyridine (Sanchez & al., J. Heterocycl. Chem. 24, 215(1987); CAS:[110919-71-6]) instead of 2-chloro-4-aminopyridine to yield [2-(5-Fluoro-6-methyl-pyridin-2-ylcarbamoyl)-6-methyl-pyridin-3-yl]-carbamic acid tert-butyl ester, white solid, MS (ISP): m/e=361.0 (M+H+). Boc-deprotection as described in example 4 step 3 yielded 3-Amino-6-methyl-pyridine-2-carboxylic acid (5-fluoro-6-methyl-pyridin-2-yl)-amide, white solid, MS (ISP): m/e=261.3 (M+H+). Palladium catalysed arylation with 3-Bromopyridine as described in example 4 step 4 yielded the final product as a yellow solid, (ISP): m/e=338.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414060B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-87fd1719c4cc435aa5d57d0014c25fc9 |
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| Source note | uspto-grants-2008_08 |
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