HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 1-Benzyl-2,3-dihydro-1H-pyrrolo[2,3-b]quinolin-4-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Aminobenzonitrile | HCID 72913 | — |
| Reactant | 2-(1-Benzyl-pyrrolidin-2-ylideneamino)benzonitrile | HCID 758406 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | 1-Benzyl-2,3-dihydro-1H-pyrrolo[2,3-b]quinolin-4-ylamine | HCID 711989 | — |
| Product | HCID 178420813 | HCID 178420813 | — |
Reaction Steps
Pyrroloquinoline compounds were synthesized as follows. The compound 1-benzyl-2,3-dihydro-1H-pyrrolo[2,3-b]quinolin-4-ylamine was prepared from the cyclization of an amidine derivative, 2-(1-benzyl-pyrrolidin-2-ylideneamino)benzonitrile, which was synthesized by condensing an anthranilonitrile and 1-benzyl-2-pyrrolidione. This compound was then reacted with potassium tert-butoxide or sodium hydride and the corresponding alkyl chloride or acyl chloride (FIG. 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06815442B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-a4925147f81146e2b5c9171157dfd38a |
| Source note | uspto-grants-2004_11 |