Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051520Generated: October 25, 2026

Ethyl bromoacetate → Ethyl 2-(2-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate

https://huagongshe.com/reaction/1051520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant2-Chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5706774—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(2-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetateHCID 8671980460%

Reaction Steps

To a solution of 2-chloro-7H-pyrrolo[2,3-d]pyrimidine (1 g, 6.54 mmol) in 25 mL THF was added t-BuOK (1.1 g, 9.81 mmol) and ethyl 2-bromoacetate (1.31 g, 7.84 mmol). The mixture was stirred and heated to reflux temperature for 2 h. After cooling the mixture was extracted with EtOAc, washed with brine, dried over Na2SO4 and concentrated to yield a crude product which was used in next step without further purification (940 mg Yield 60%). LCMS (m/z): 240.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388173B2
Source datasetuspto-grants-2016_07
ORD IDord-4beddd233ff74301a1a8c86918cba51d
Source noteuspto-grants-2016_07