HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502800Generated: October 26, 2026
Dimethylformamide → N-(3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)phenyl)acetamide
https://huagongshe.com/reaction/502800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | N-[4-(2-amino-5-nitro-pyridin-3-ylethynyl)-phenyl]-acetamide | HCID 68462435 | — |
| Product | N-(3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)phenyl)acetamide | HCID 68462732 | 68% |
Reaction Steps
Potassium tert-butoxide (2.25 g, 20 mmol) was added to a solution of N-[4-(2-amino-5-nitro-pyridin-3-ylethynyl)-phenyl]-acetamide (1.48 g, 5 mmol) in a 2:1 mixture of tetrahydrofuran and dimethylformamide (75 mL). The mixture was heated at 70° C. for 16 hours then the tetrahydrofuran was removed in vacuo. The mixture was poured onto a pad of silica and eluted with 10% methanol in ethyl acetate. The organics were concentrated in vacuo to 5% of their original volume and water (30 mL) was added. The resultant orange solid was filtered and dried to afford N-[3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)-phenyl]-acetamide (1.01 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776878B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-2e4c0ac1435a484f98c22a459d2edea3 |
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| Source note | uspto-grants-2010_08 |
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