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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854407Generated: November 2, 2026

Hydrochloric Acid → (5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)methanol

https://huagongshe.com/reaction/1854407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant5-tosyl-5H-pyrrolo[2,3-b]pyrazine-2-carbaldehydeHCID 58009883—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
Product(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)methanolHCID 5801002595%

Reaction Steps

To a solution of 5-tosyl-5H-pyrrolo[2,3-b]pyrazine-2-carbaldehyde (37.6 g, 125 mmol) in EtOH (500 mL) and 1,4-dioxane (500 mL) was added NaBH4 (4.72 g, 125 mmol) in one portion. After about 3 h, aqueous HCl (1N, 400 mL) was slowly added to the reaction mixture. The mixture was concentrated to one-half the original volume under reduced pressure and EtOAc (1000 mL) and water (500 mL) were added to the mixture. The layers were separated and the aqueous layer was extracted with EtOAc (500 mL). The combined organic layers were dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to provide (5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)methanol (35.9 g, 95% yield) as a tan solid: LC/MS (Table 2, Method a) Rt=1.97 min; MS m/z: 304 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962629B2
Source datasetuspto-grants-2015_02
ORD IDord-a3e71ddb9fc147bba685778be8582c6c
Source noteuspto-grants-2015_02