HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1'-Carbonyldiimidazole → NGB 2904 hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 9H-fluorene-2-carboxylic acid | HCID 348591 | — |
| Reactant | 1-Piperazinebutanamine, 4-(2,3-dichlorophenyl)- | HCID 11098669 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | NGB 2904 hydrochloride | HCID 19366304 | 139.4% |
Reaction Steps
A mixture of 9H-fluorene-2-carboxylic acid (100 mg, 0.48 mmol) and 1,1'-carbonyldiimidazole (80 mg, 0.5 mmol) in 10 mL of anhydrous tetrahydrofuran was stirred for 8 hours. A solution of 4-[4-(2,3-dichlorophenyl)-1-piperazinyl]-1-aminobutane (150 mg, 0.5 mmol) in 1 mL of tetrahydrofuran was added and the resulting mixture was stirred for 30 minutes. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with aqueous Na2CO3 solution, dried (Na2SO4) and concentrated in vacuo to give the title compound (185 mg, 78%). Hydrochloride salt was prepared lay treating the free base with a solution of hydrogen chloride in ethyl acetate (top 262-4° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05659033 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-385f0161e99f4bf781a4ae6f4f2e7f7f |
| Source note | uspto-grants-1997_08 |