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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051765Generated: October 31, 2026

N-bromobutanimide → 5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1051765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5380710—

Reaction Steps

[To a suspension of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (F-1) (3.99 g, 26.0 mmol, 1.0 eq) in anhydrous DCM (150 mL) under argon, N-bromosuccinimide (6.02 g, 33.8 mmol, 1.3 eq) is added and the resulting mixture is stirred at RT for 3 h. The reaction mixture is diluted with MeOH (30 mL) and then concentrated in vacuo. The residue is triturated with H2O (150 mL). This is collected by filtration and then re-crystallized in MeOH to afford the product, 5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (G-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388183B2
Source datasetuspto-grants-2016_07
ORD IDord-9d5e2c9158eb464395bb6ffeee7f4e96
Source noteuspto-grants-2016_07