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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382013Generated: October 25, 2026

N,N-Diethyl-2-propanamine → 2-Pyridin-2-yl-pyrimidine-5-carboxylic acid pyrrolo[2,3-b]pyridine-1-ylamide

https://huagongshe.com/reaction/2382013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Diethyl-2-propanamineHCID 521913—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant1H-Pyrrolo[2,3-b]pyridin-1-amineHCID 5223950—
Reactant2-(Pyridin-2-yl)pyrimidine-5-carboxylic acidHCID 24903633—
SolventDimethylformamideHCID 6228—
Product2-Pyridin-2-yl-pyrimidine-5-carboxylic acid pyrrolo[2,3-b]pyridine-1-ylamideHCID 5919995732.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

Diethyl-iso-propylamine (1.13 mmol) is added a solution of 2-pyridin-2-yl-pyrimidine-5-carboxylic acid (0.75 mmol), pyrrolo[2,3-b]pyridine-1-ylamine (0.75 mmol) and TBTU in anhydrous DMF (7 mL) at rt, and the reaction mixture is stirred at 80° C. overnight. The reaction mixture is concentrated in vacuo. The residue is dissolved in EtOAc, washed with water twice, dried (Na2SO4), filtered and concentrated in vacuo. The residue is purified by silica gel chromatography eluting with 10% MeOH in DCM to give a crude product. The product is crystallized from EtOAc to afford 2-pyridin-2-yl-pyrimidine-5-carboxylic acid pyrrolo[2,3-b]pyridine-1-ylamide (78 mg, 25%) as a solid. MS: 317 (M+H); 1H NMR (300 MHz, CD3OD): δ 6.56 (m, H) 7.24 (m, H), 7.53 (m, H), 7.61 (m, H), 8.01-8.17 (m, 2H), 8.27 (d, H), 8.69 (m, H), 8.78(m, H), 9.51 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-4661879e8fd548988b4677d5f4fb56c8
Source noteuspto-grants-2012_09