HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-(1,4-Diazabicyclo[3.2.2]nonan-4-yl)-5-nitroisonicotinic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)5-nitroisonicotinate | HCID 67114669 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1,4-Diazabicyclo[3.2.2]nonan-4-yl)-5-nitroisonicotinic acid | HCID 67114923 | 55.6% |
Reaction Steps
To a solution of methyl 2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)5-nitroisonicotinate (Intermediate 27A) (6.0 g, 19.6 mmol) in tetrahydrofuran (15 mL) under nitrogen was added lithium hydroxide (2.47 g, 58.8 mmol), methanol (10 mL) and water (15 mL), reaction then stirred overnight. The reaction mixture was concentrated and purified by a 50 g silica column eluting with 10-40% methanol in DCM to afford 2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-5-nitroisonicotinic acid (3.2 g, 10.9 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841289B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-f434d5185f954e179a7907e89f88bdb7 |
| Source note | uspto-grants-2014_09 |