HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenoxybenzoyl chloride → N-[2-(6-Bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-1-cyano-1-methylethyl]-4-phenoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenoxybenzoyl chloride | HCID 74193 | — |
| Reactant | 2-Amino-3-(6-bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-2-methylpropionitrile | HCID 66620126 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[2-(6-Bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-1-cyano-1-methylethyl]-4-phenoxybenzamide | HCID 68706734 | — |
Reaction Steps
Using a procedure similar to that described in Example 60, except using a solution of 4-phenoxybenzoyl chloride (0.16 mmole) in THF and a solution of 2-amino-3-(6-bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-2-methylpropionitrile (0.075 mmole, described in Example 182) in THF mixed with TEA (3% v./v.), the title compound was isolated as solid residue (6.7 mg). It was dissolved in DMSO for further biological evaluation and analyzed by LCMS. MS (ES): M/Z [M+H]=476, RT=0.63 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461176B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-527d0470645347c5a20398fb166ee7c0 |
| Source note | uspto-grants-2013_06 |