HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414742Generated: October 31, 2026
HCID 21956178, compound → 6-Chloro-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one
https://huagongshe.com/reaction/2414742
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 21956178 | HCID 21956178 | — |
| Reactant | HCID 21956193 | HCID 21956193 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 6-Chloro-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one | HCID 21907047 | — |
Reaction Steps
A solution of 2.36 g (7.26 mmol) of the mixture of 3,3-dibromo-6-chloro-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one and 3,3,5-tribromo-6-chloro-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one in THF (70 mL) and saturated ammonium chloride solution (70 mL) was treated with, 6 g (92 mmol) of powdered zinc. The mixture was stirred for 2 h, and another 6 g (92 mmol) portion of zinc was added. Stirring was continued another 2 h. The zinc was filtered off and washed with ether. The ether phase was separated, and the aqueous phase was extracted twice with a 1:1 mixture of THF/ether. The combined organic extracts were dried over magnesium sulfate, filtered and concentrated. The crude residue was loaded onto 7.5 g of silica gel and chromatographed on silica gel, eluting with a 90% hexane/10% ethyl acetate to 66% hexane/33% ethyl acetate gradient to give 0.647 g of the title compound. 1H NMR (DMSO-d6): δ 3.57 (s, 2H), 7.04 (d, J=7.6 Hz, 1H), 7.61 (d, J=7.6 Hz, 1H), 11.2 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06815439B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-6ac042b3acf54c5d94683b0c19ec4c77 |
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| Source note | uspto-grants-2004_11 |
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