HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malononitrile → HCID 10345146, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Bromo-4,5-dimethoxybenzaldehyde | HCID 81379 | — |
| Reactant | HCID 85887666 | HCID 85887666 | — |
| Reactant | HCID 86604976 | HCID 86604976 | — |
| Product | HCID 10345146 | HCID 10345146 | — |
Reaction Steps
2-Amino-4-(3-bromo-4,5-dimethoxyphenyl)-3-cyano-7-oxiranyl-methyl-4H-pyrrolo[2,3-h]chromene: The title compound was prepared from 1-oxiranylmethyl-4-hydroxy-indole (70 mg, 0.37 mmol), 5-bromoveratraldehyde (91 mg, 0.37 mmol), malononitrile (25 mg, 0.37 mmol) and piperidine (0.01 mL, 0.18 mmol), similar to Example 16, to yield 80 mg (45%) of a white solid. 1H NMR (CDCl3): 7.15 (dd, J=1.5 Hz, 1H), 7.10 (dd, J=2.7 Hz, 1H), 6.92-6.91 (m, 1H), 6.78-6.75 (m, 2H), 6.62 (dd, J=0.9 Hz, 1H), 4.77 (s, 1H), 4.70 (brs, 2H), 4.48-4.43 (m, 1H), 4.15-4.13 (m, 1H), 3.83 (s, 3H), 3.82 (s, 3H), 3.28-3.27 (m, 1H), 2.84-2.81 (m, 1H), 2.48-2.44 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07528164B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-a28beba0885d49f5a98253ed10d9b088 |
| Source note | uspto-grants-2009_05 |