HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 6-Chloro-1H-pyrrolo[2,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (6-Chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)(phenyl)methanone | HCID 15013892 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Chloro-1H-pyrrolo[2,3-b]pyridine | HCID 11344118 | — |
Reaction Steps
A solution of (Intermediate C3) (3.12 mmol) in MeOH (90 mL) was treated with 1 M NaOH (30 mL) at rt for 18 h. The solution was freed of MeOH under reduced pressure and ethyl acetate was added to the aqueous layer. The aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with sat. NaHCO3, and dried over Na2SO4. The mixture was filtered and the solvent was evaporated to give a solid 6-chloro-1H-pyrrolo[2,3-b]pyridine (Intermediate C4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07399868B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-12104a8f793c40f4a9680a0d47d24369 |
| Source note | uspto-grants-2008_07 |