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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888160Generated: November 1, 2026

Methanol → 2-((1H-pyrrolo[2,3-b]pyridin-3-yl)methylamino)nicotinic acid

https://huagongshe.com/reaction/888160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Aminonicotinic acidHCID 72930—
ReactantSodium borohydrideHCID 4311764—
Reactant1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-((1H-pyrrolo[2,3-b]pyridin-3-yl)methylamino)nicotinic acidHCID 69265593—

Reaction Steps

2-Aminonicotinic acid (945 mg, 6.85 mmol) was added to a suspension of 1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde (1 g, 6.85 mmol) in toluene (10 mL) under N2 atmosphere. A catalytic amount of tosyl acid was added to above and the mixture was heated to reflux for 3 h. The reaction was cooled to RT and NaBH4 was added. After stirring for 10 min., MeOH (2 ml) was added to above and the reaction was stirred for another 5 h at RT. The mixture was diluted with water and extracted with EtOAc. The aq layer was acidified using 1N HCl. The resultant precipitate was filtered and washed with AcCN affording compound as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247556B2
Source datasetuspto-grants-2012_08
ORD IDord-15373312f5d04da7956296e9c88cb035
Source noteuspto-grants-2012_08