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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571729Generated: October 31, 2026

Bromoacetyl bromide → 1-(2-benzyloxy-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazin-5-yl)-2-bromo-ethanone

https://huagongshe.com/reaction/571729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
Reactant2-(Benzyloxy)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazineHCID 86706492—
SolventDichloromethaneHCID 6344—
Product1-(2-benzyloxy-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazin-5-yl)-2-bromo-ethanoneHCID 86706496—

Reaction Steps

A solution of 2-(benzyloxy)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine (0.02 g, 0.087 mmol) in a DCM (1 mL) was treated with bromoacetyl bromide (7.6 μL, 17.6 mg, 0.087 mmol) at 0° C. The solvents were evaporated in vacuo to yield 1-(2-benzyloxy-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazin-5-yl)-2-bromo-ethanone as a white solid, that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029366B2
Source datasetuspto-grants-2015_05
ORD IDord-8177760a94774f5fa09f57182d8e0aaf
Source noteuspto-grants-2015_05