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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-[4-(2-amino-5-nitro-pyridin-3-ylethynyl)-phenyl]-acetamideHCID 68462435—
ProductN-(3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)phenyl)acetamideHCID 6846273268%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776878B2
Source datasetuspto-grants-2010_08
ORD IDord-2e4c0ac1435a484f98c22a459d2edea3
Source noteuspto-grants-2010_08