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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766153Generated: November 2, 2026

1H-Pyrrolo(2,3-b)pyridine → HCID 21110056, compound

https://huagongshe.com/reaction/1766153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
ReactantSodium hydrideHCID 24758—
ReactantIsoquinoline, 1-chloro-HCID 140539—
SolventDimethylformamideHCID 6228—
ProductHCID 21110056HCID 2111005652.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

0.894 g of 60% sodium hydride (37.25 mmol) was added with stirring to 20 cm3 of dimethylformamide under an argon atmosphere at a temperature in the region of 20° C. and then a solution of 4 g (33.86 mmol) of 1H-pyrrolo[2,3-b]pyridine in 20 cm3 of dimethylformamide was gradually added. After stirring at a temperature in the region of 20° C. for 30 minutes, a solution of 5.816 g (35.55 mmol) of 1-chloroisoquinoline in 20 cm3 of dimethylformamide was added and then the reaction mixture was heated at a temperature in the region of 100° C. for 15 h. After concentrating to dryness under reduced pressure (2.7 kPa), the residue was taken up in 2 times 50 cm3 of water. The residual oil was taken up in 30 cm3 of diethyl ether. The white crystals that formed were filtered off and then dried under reduced pressure (2.7 kPa) at a temperature in the region of 20° C. 4.36 g of 1-(isoquinolin-1-yl)-1H-pyrrolo[2,3-b]pyridine were thus obtained in the form of an off-white solid melting at 87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230007B2
Source datasetuspto-grants-2007_06
ORD IDord-8ed82a29e5ec4263b87a7958abc482f9
Source noteuspto-grants-2007_06