HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-2-phenyl-oxazole-4-carboxylic acid → 5-Chloro-2-phenyl-oxazole-4-carboxylic acid [6-(acetyl-methyl-amino)-pyridin-3-yl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-2-phenyl-oxazole-4-carboxylic acid | HCID 59301278 | — |
| Reactant | N-(5-aminopyridin-2-yl)-N-methylacetamide | HCID 59301435 | — |
| Product | 5-Chloro-2-phenyl-oxazole-4-carboxylic acid [6-(acetyl-methyl-amino)-pyridin-3-yl]-amide | HCID 59301454 | — |
Reaction Steps
With a procedure similar to example 16 above, 5-chloro-2-phenyl-oxazole-4-carboxylic acid [6-(acetyl-methyl-amino)-pyridin-3-yl]-amide was prepared from 5-chloro-2-phenyl-oxazole-4-carboxylic acid and N-(5-amino-pyridin-2-yl)-N-methyl-acetamide. LCMS calcd for C18H15ClN4O3 (m/e) 370, obsd 371 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714126B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-26f2a635f4254db39f34476f08d2adc4 |
| Source note | uspto-grants-2010_05 |