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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905994Generated: October 30, 2026

Sodium hydride → 2-Bromo-7-methyl-5-[[2-(trimethylsilyl)ethoxy]methyl]-5H-pyrrolo[2,3-b]pyrazine

https://huagongshe.com/reaction/905994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
ReactantHCID 86642308HCID 86642308—
SolventDimethylformamideHCID 6228—
Product2-Bromo-7-methyl-5-[[2-(trimethylsilyl)ethoxy]methyl]-5H-pyrrolo[2,3-b]pyrazineHCID 8664230977%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Bromo-7-methyl-5H-pyrrolo[2,3-b]pyrazine (0.279 g, 1.321) was dissolved in DMF (5 mL) and cooled down to 0° C. NaH (60%, 63 mg, 1.58 mmol) was added slowly. After the addition was complete stirring was continued for 30 minutes at 0° C. (2-Chloromethoxy-ethyl)-trimethyl-silane (0.28 mL, 1.58 mmol) was added and the reaction mixture was allowed to warm up overnight. The reaction was quenched with H2O. The aqueous layer was extracted with EtOAc. The organic layer was dried (MgSO4), filtered, concentrated, and purified by SiO2 chromatography (24 g SiO2, hexanes/EtOAc 0-35% EtOAc) to give 340 mg of 2-bromo-7-methyl-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine as a yellow liquid (77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012974B2
Source datasetuspto-grants-2011_09
ORD IDord-de6937adf45b4d69bd3915e8f660c527
Source noteuspto-grants-2011_09