HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrimidine-5-carboxaldehyde → HCID 178513983, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrimidine-5-carboxaldehyde | HCID 2761034 | — |
| 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 178513983 | HCID 178513983 | 14.3% |
Reaction Steps
In a similar fashion to Compound LXXXVII, (1S,2S,3R,4R)-3-(2,3-Diamino-5-bromo-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide (50 mg, 0.148 mmol) and Pyrimidine-5-carbaldehyde (17.6 mg, 0.163 mmol) were reacted to produce 9.0 mg (14%) of the title compound. mp: >300° C., 1H NMR (300 MHz, DMSO-d6): 13.7 (s, 1H), 9.42 (s, 2H), 9.28 (s, 1H), 8.10 (s, 1H), 7.77 (s, 1H), 7.35 (m, 1H), 7.23 (s, 1H), 6.39 (d, J=8 Hz, 1H), 5.22 (t, J=8 Hz, 1H), 3.3 (s, 1H), 2.90 (s, 1H), 2.78 (s, 1H), 2.63 (d, J=8 Hz, 1H), 2.25 (d, J=8 Hz, 1H), 1.40 (d, J=9 Hz, 1H). MS: 426, 428 (M+H), HPLC: 1.91 min (G method).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238656B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-524dae150e1241f9b03906e176801c58 |
| Source note | uspto-grants-2016_01 |