HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Cyclopropyl-6-cyclopropylmethoxy-pyridine-2-carboxylic acid → 5-Cyclopropyl-N-(cyclopropyl(5-methyl-1,2,4-oxadiazol-3-yl)methyl)-6-(cyclopropylmethoxy)picolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Cyclopropyl-6-cyclopropylmethoxy-pyridine-2-carboxylic acid | HCID 71087346 | — |
| Reactant | (S)-2-Cyclopropyl-1-(5-methyl-[1,2,4]oxadiazol-3-yl)-ethylamine | HCID 86674748 | — |
| Reactant | Cyclopropyl-(5-methyl-[1,2,4]oxadiazol-3-yl)-methylamine | HCID 86674778 | — |
| Product | 5-Cyclopropyl-N-(cyclopropyl(5-methyl-1,2,4-oxadiazol-3-yl)methyl)-6-(cyclopropylmethoxy)picolinamide | HCID 71087853 | — |
Reaction Steps
The title compound was synthesized in analogy to Example 1, using 5-cyclopropyl-6-cyclopropylmethoxy-pyridine-2-carboxylic acid (Example 42 a) and cyclopropyl-(5-methyl-[1,2,4]oxadiazol-3-yl)-methylamine (which can e.g. be prepared in a similar manner than (S)-2-cyclopropyl-1-(5-methyl-[1,2,4]oxadiazol-3-yl)-ethylamine (Example 38 e)) as starting materials, MS (EI): m/e=369.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290451B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-e6de360cfffd48bca2e95764c5dbab28 |
| Source note | uspto-grants-2016_03 |