HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Pyridinecarboxaldehyde → HCID 70795706, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Reactant | 3-(1H-Pyrrolo[2,3-b]pyridin-4-ylamino)-thiophene-2-carboxylic acid [2-(4-methoxy-benzylamino)-ethyl]-amide | HCID 50924451 | — |
| Product | HCID 70795706 | HCID 70795706 | — |
Reaction Steps
This compound was prepared in an analogous manner as 3-(1H-Pyrrolo[2,3-b]pyridin-4-ylamino)-thiophene-2-carboxylic acid [2-(4-methoxy-benzylamino)-ethyl]amide using 3-pyridinecarboxaldehyde instead of 4-methoxy benzaldehyde. LCMS (ESI) 393 (M+H) 1H NMR (400 MHz, METHANOL-d4) δ ppm 8.51 (1H, d, J=2.20 Hz) 8.39 (1H, dd, J=4.91, 1.54 Hz) 8.00 (1H, d, J=5.66 Hz) 7.80 (1H, dt, J=7.83, 1.87 Hz) 7.64 (1H, d, J=5.42 Hz) 7.47 (1H, d, J=5.47 Hz) 7.33 (1H, dd, J=7.83, 4.91 Hz) 7.24 (1H, d, J=3.56 Hz) 6.87 (1H, d, J=5.66 Hz) 6.55 (1H, d, J=3.56 Hz) 3.80 (2H, s) 3.51 (2H, t, J=6.30 Hz) 2.79 (2H, t, J=6.22 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023847B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-7bbd75a111da46778fc22f1c91a8cc48 |
| Source note | uspto-grants-2015_05 |