HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile → 5-amino-N-[5-[(5R)-5-amino-3,3-difluoro-azepan-1-yl]-1-methyl-pyrazol-4-yl]-2-(6-cyano-2-pyridyl)thiazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile | HCID 17750468 | — |
| Reactant | tert-butyl N-[2-bromo-4-[[5-[(5R)-5-(tert-butoxycarbonylamino)-3,3-difluoro-azepan-1-yl]-1-methyl-pyrazol-4-yl]carbamoyl]thiazol-5-yl]carbamate | HCID 86680147 | — |
| Product | 5-amino-N-[5-[(5R)-5-amino-3,3-difluoro-azepan-1-yl]-1-methyl-pyrazol-4-yl]-2-(6-cyano-2-pyridyl)thiazole-4-carboxamide | HCID 74983276 | — |
Reaction Steps
Following the procedures in Example 428, tert-butyl N-[2-bromo-4-[[5-[(5R)-5-(tert-butoxycarbonylamino)-3,3-difluoro-azepan-1-yl]-1-methyl-pyrazol-4-yl]carbamoyl]thiazol-5-yl]carbamate was reacted with 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carbonitrile to give 461. LCMS (ES+) m/z 474 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08614206B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-26a4aeba265d42758c3760b4244b1a16 |
| Source note | uspto-grants-2013_12 |