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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051769Generated: October 27, 2026

Carbon Dioxide → 4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carboxylic acid

https://huagongshe.com/reaction/1051769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5380710—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carboxylic acidHCID 22460866—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixture of 5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (G-1) (6.24 g, 26.8 mmol, 1.0 eq) in anhydrous THF (100 mL) at −78° C. under argon, n-BuLi solution (2.5 M in THF, 23.6 mL, 59.0 mmol, 2.2 eq) is added dropwise over 30 min. The reaction mixture is stirred at −78° C. for 1 h and then dry ice (300 g) is added in portions under an argon atmosphere. The resulting mixture is allowed to warm to RT and then stirred at RT overnight. The reaction mixture is diluted with H2O (200 mL) and extracted with ethyl acetate (50 mL×4). The aqueous layer is acidified with conc. HCl to adjust the pH to 3-4. The precipitate is collected by filtration, rinsed with H2O (30 mL) and dried in vacuo to afford the product, 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid (H-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388183B2
Source datasetuspto-grants-2016_07
ORD IDord-3c1f556fb6434853be7d42b3473a1773
Source noteuspto-grants-2016_07