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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381648Generated: November 1, 2026

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

https://huagongshe.com/reaction/2381648

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 numberUS08258144B2
Source datasetuspto-grants-2012_09
ORD IDord-0dd663ebc94447c5b0128695adac2d4c
Source noteuspto-grants-2012_09