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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281422Generated: October 26, 2026

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

https://huagongshe.com/reaction/2281422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidineHCID 14116871—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5799044095%

Reaction Steps

To a suspension of 2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine (105 mg, 0.560 mmol) in CH2Cl2 (7 mL) at room temperature, NBS (109 mg, 0.610 mmol) was added. The mixture was stirred at room temperature for 18 h. CH2Cl2 was removed in vacuo. The residue was partitioned between water and EtOAc. The organic phase was separated, washed with 5% NaHCO3, dried over Na2SO4, concentrated in vacuo to give 5-bromo-2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine (142 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139581B2
Source datasetuspto-grants-2015_09
ORD IDord-45b6e93bce4e4bb3980280715d11828b
Source noteuspto-grants-2015_09