HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-chloropyridine → HCID 21906417, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-chloropyridine | HCID 66174 | — |
| Reactant | HCID 21906617 | HCID 21906617 | — |
| Reactant | HCID 131726014 | HCID 131726014 | — |
| Product | HCID 21906417 | HCID 21906417 | — |
Reaction Steps
Using methods substantially equivalent to those described in Example 51-D, 2-[(1-Boc-piperidin-4-ylcarbonyl)amino]-N-(5-chloropyridin-2-yl)-5-(N,N-dimethylaminosulfonylbenzamide (0.912 g, 85%) was prepared from 2-(1-Boc-piperidin-4-yl)-6-(N,N-dimethylaminosulfonyl)-4H-3,1-benzoxazin-4-one and 2-amino-5-chloropyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129245B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-bc41a546f806433cb1631c675836be15 |
| Source note | uspto-grants-2006_10 |