HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Azaindole → HCID 67447567, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Azaindole | HCID 9219 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67447567 | HCID 67447567 | — |
Reaction Steps
A solution of 1H-pyrrolo[2,3-c]pyridine (10 mmol) in DMF cooling on an ice bath was treated with NaH (143 mmol). After stirred at room temperature for thr iodopropane (26 mmol) was added dropwise. The mixture was allowed to react at room temperature for further 3 hrs. Upon cooling on an ice bath the mixture was quenched with 20 mL H2O, followed by extraction with diethyl ether (5×50 mL). The organic layers were combined, washed with brine, dried on MgSO4 and filtered. The solvent was evaporated and dried on a high vacuum to give 1-propyl-1H-pyrrolo[2,3-c]pyridine as orange oil. MS (ESI+) m/z 161.1063 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309550B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-3d08893f29544649810cc6b74c8c2f00 |
| Source note | uspto-grants-2012_11 |