HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-azabicyclo[3.3.1]nonane → HCID 10474387, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-azabicyclo[3.3.1]nonane | HCID 42603 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18146450 | HCID 18146450 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 10474387 | HCID 10474387 | — |
Reaction Steps
A solution of 4-fluoro-N-quinolin-3-yl-benzamide (0.080 g, 0.299 mmol), 3-aza-bicyclo[3.3.1]nonane (0.200 g, 1.60 mmol) and N,N-diisopropylethylamine (0.10 mL, 0.57 mmol) in dimethyl sulfoxide (2 mL) was heated to 100° C. for 11 days. The DMSO solution was applied to a preparative reverse phase C18 column, and the product was eluted with a gradient of acetonitrile in water with 0.1% trifluoroacetic acid, to give the product as a trifluoroacetate salt, a yellow solid, 0.065 g (36%). MS: m/z 372 (MH+). 1H NMR (DMSO-d6): 1.40-1.50 (m, 1 H), 1.58-1.93 (m, 7 H), 2.05 (br s, 2 H), 3.04-3.08 (m, 2 H), 3.85 (d, 2 H), 7.00 (d, 2 H), 7.62-7.76 (m, 2 H), 7.96 (d, 2 H), 8.02 (d, 2 H), 8.95 (d, 1 H), 9.28 (d, 1 H) and 10.45 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394828B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-54dd711b917444e5bffd48298e33fe01 |
| Source note | uspto-grants-2013_03 |