Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 3-(1h-pyrazol-1-yl)benzaldehyde | HCID 7172309 | — |
| Reactant | (1S,2S,3R,4R)-3-(2,3-Diamino-5-chloro-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide | HCID 117701912 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178513992 | HCID 178513992 | — |
Reaction Steps
(1S,2S,3R,4R)-3-(2,3-Diamino-5-chloro-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide (50.00 mg, 0.1702 mmol), 3-Pyrazol-1-yl-benzaldehyde (32.2 mg, 0.187 mmol), and Ammonium acetate (26.2 mg, 0.340 mmol) were combined in Ethanol (2.21 mL, 37.8 mmol) in a reaction tube and heated at 80° C. overnight. Upon cooling, a precipitate formed. Reaction was diluted with 3 ml ethyl ether and cooled in an ice/water bath. The resulting solid was filtered, washed with cold ether and dried under hi-vacuum. Product is a white solid. Yield: 41.35 mg (54%) of the title compound. (300 MHz, DMSO-d6) 13.39 (s, 1H), 8.68 (s, 1H), 8.53 (s, 1H), 8.06 (d, J=7.6 Hz, 1H), 7.98 (s, 1H), 7.93 (d, J=8 Hz, 1H), 7.81 (m, 2H), 7.67 (t, J=16 Hz, 8 Hz, 1H), 7.32 (d, J=8 Hz, 1H), 7.25 (s, 1H), 6.62 (s, 1H), 6.53 (s, 1H), 6.39 (s, 1H), 5.15 (t, J=17 Hz, J=9 Hz, 1H), 2.89 (d, J=17 Hz, 2H), 2.63 (d, J=8 Hz, 1H), 2.24 (d, J=8 Hz, 1H), 1.39 (d, J=8 Hz, 1H). MS=446 (M+H), HPLC: 2.51 min. (G Method)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09238656B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-e797c97ea20d477194cf9d0fdb7ce72e |
|---|
| Source note | uspto-grants-2016_01 |
|---|