HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Pyridineacetic acid → HCID 12999592, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Pyridineacetic acid | HCID 108 | — |
| Reactant | Methoxy-methyl amide | HCID 53630747 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 12999592 | HCID 12999592 | — |
Reaction Steps
In another example of the general procedure (scheme 2), readily available pyridin-3-yl-acetic acid (10) is converted to the N-methyl-N-methoxyamide derivate (12), which is reacted with BuLi to produce 1-pyridin-3-yl-hexan-2-one (13). N,N-dimethylformamide dimethylacetal treatment of 13 furnished the enamine (14) which is converted to the pyrazol (15). The synthesis of 3-(4-Butyl-1H-pyrazol-3-yl)-1,2,5,6-tetrahydro-1-methylpyridine (16) is illustrated in scheme 2 according to the two step sequence shown in scheme 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084473B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-c7300da0306f4503aa3ababc126f085b |
| Source note | uspto-grants-2011_12 |