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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910873Generated: October 27, 2026

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

https://huagongshe.com/reaction/1910873

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 (E-2) (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 then 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 then diluted with H2O (200 mL) and extracted with ethyl acetate (50 mL×4). The aqueous layer is acidified with con. HCl to adjust the pH to 3-4. The precipitate is then 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 (G-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604032B2
Source datasetuspto-grants-2013_12
ORD IDord-f8e0b122084a4bf3926c45f2351d34f2
Source noteuspto-grants-2013_12