HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 2-Amino-6-chloro-N-methoxy-N-methyl-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2,6-Dichloro-N-methoxy-N-methylpyridine-3-carboxamide | HCID 53403411 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Amino-6-chloro-N-methoxy-N-methyl-nicotinamide | HCID 58590824 | 8% |
Reaction Steps
2,6-Dichloro-N-methoxy-N-methyl-nicotinamide (202.4 mg, 0.8610 mmol, Example 1) and concentrated ammonium hydroxide (1.8 mL, 29.4%, Fisher) in tetrahydrofuran (2.5 mL) were heated to 155° C. in the microwave for 2 hr. The reaction mixture was concentrated and the residue was purified on silica gel with hexanes/ethyl acetate to give 2-Amino-6-chloro-N-methoxy-N-methyl-nicotinamide (14.3 mg, 8% yield). HRMS, observed: 215.0463, Calcd for M+: 215.0462.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07423051B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-2252cf8254b348ab8f83890ebf6412be |
| Source note | uspto-grants-2008_09 |