HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexamethylenetetramine → 4-fluoro-1-(3-methoxypropyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1H-Pyrrolo[2,3-b]pyridine, 4-fluoro-1-(3-methoxypropyl)- | HCID 59494223 | — |
| Product | 4-fluoro-1-(3-methoxypropyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde | HCID 59494169 | — |
Reaction Steps
A solution of 4-fluoro-1-(3-methoxypropyl)-1H-pyrrolo[2,3-b]pyridine (520 mg) and hexamethylenetetramine (700 mg) in trifluoroacetic acid (9.1 ml) was stirred at 80° C. for 4 hours. After evaporation of the solvent in vacuo, the resulted residue was dissolve in ethyl acetate. The solution was poured slowly into a saturated aqueous solution of sodium bicarbonate and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and concentrated in vacuo. The resulted residue was purified with a silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=60/40 to 20/80) to give 4-fluoro-1-(3-methoxypropyl)-1H-pyrrolo[2,3-b]pyridin-3-carbaldehyde (260 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975252B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-ba5ca38261e04879b00715588723f4db |
| Source note | uspto-grants-2015_03 |