HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanobenzaldehyde → HCID 178509628, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | (1S,2S,3R,4R)-3-(2,3-Diamino-5-bromo-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide | HCID 117701905 | — |
| Product | HCID 178509628 | HCID 178509628 | 47.6% |
Reaction Steps
In a similar fashion to Compound CXXV, (1S,2S,3R,4R)-3-(2,3-Diamino-5-bromo-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide (75 mg, 0.22 mmol), 4-Formylbenzonitrile (32.0 mg, 0.244 mmol), and Ammonium acetate (34.2 mg, 0.444 mmol) were reacted to produce 47.01 mg (47%) of the title compound. (300 MHz, DMSO-d6) 13.60 (s, 1H), 8.29 (d, J=8 Hz, 2H), 8.08 (s, 1H), 7.76 (s, 1H), 7.31 (m, 1H), 7.24 (s, 1H), 6.42 (m, 1H), 6.37 (m, 1H), 5.20 (t, J=17 Hz, 8.5 Hz, 1H), 2.90 (s, 1H), 2.79 (s, 1H), 2.62 (d, J=8 Hz, 1H), 2.24 (d, J=8 Hz, 1H), 1.38 (d, J=8 Hz, 1H). MS=451 (M+H), HPLC: 2.43 min. (G Method)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238656B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-4b60f22c281f491a8aff6c6eaf762c74 |
| Source note | uspto-grants-2016_01 |