HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(4-methyl-5-nitropyridin-2-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Amino-4-methyl-5-nitropyridine | HCID 243165 | — |
| Product | N-(4-methyl-5-nitropyridin-2-yl)acetamide | HCID 13567013 | — |
Reaction Steps
4-Methyl-5-nitro-pyridin-2-ylamine (1.0 g) was treated with acetic anhydride according to General Procedure Y to give N-(4-Methyl-5-nitro-pyridin-2-yl)-acetamide (1.1 g). LCMS (m/z): 196. N-(4-Methyl-5-nitro-pyridin-2-yl)acetamide (0.5 g) was reduced under hydrogen atmosphere according to General Procedure Z to give N-(5-Amino-4-methyl-pyridin-2-yl)-acetamide (0.4 g), LCMS (m/z): 166. This was converted to 6-acetylamino-4-methyl-pyridine-3-sulfonyl chloride (0.35 g) according to General Procedure AA. LCMS (m/z): 249.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987295B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-4c76b1ae96b948a2be5c70de633b7e2c |
| Source note | uspto-grants-2015_03 |