HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dihydro-2H-pyrrolo(2,3-b)pyridin-2-one → HCID 178517367, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dihydro-2H-pyrrolo(2,3-b)pyridin-2-one | HCID 13864095 | — |
| Reactant | HCID 86651961 | HCID 86651961 | — |
| Product | HCID 178517367 | HCID 178517367 | 28.2% |
Reaction Steps
The title compound (7 mg, 21%) was synthesized as yellow solid according to the method described for Example A67 using 1H-pyrrolo[2,3-b]pyridin-2(3H)-one (9.3 mg, 0.07 mmol) and (E)-3-(2-(pyridin-2-yl)vinyl)-1H-indazole-6-carbaldehyde (17 mg, 0.068 mmol). 1H NMR (400 MHz, DMSO-d6) δ 13.53 (s, 1H, NH), 11.27 (s, 1H, NH), 8.62 (d, J=4.0 Hz, 1H), 8.35 (d, J=8.4 Hz, 1H), 8.12 (d, J=5.2 Hz, 1H), 8.02-7.89 (m, 4H), 7.82 (t, J=8.0 Hz, 1H), 7.69 (d, J=7.6 Hz, 1H), 7.63 (d, J=16.8 Hz, 1H), 7.56 (d, J=8.4 Hz, 1H), 7.28 (t, J=6.0 Hz, 1H), 6.91 (dd, J=7.6 Hz, 5.6 Hz, 1H); MS ESI 366.1 [M+H]+, calcd for [C22H15N5O+H]+ 366.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765748B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-5630e292273c47a0bf7c246e18608d71 |
| Source note | uspto-grants-2014_07 |