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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961713Generated: October 28, 2026

Sodium borohydride → HCID 59570676, compound

https://huagongshe.com/reaction/1961713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59570680HCID 59570680—
SolventMethanolHCID 887—
ProductHCID 59570676HCID 5957067680%

Reaction Steps

Sodium borohydride (25 mg, 0.66 mmol) was added to an ice cooled solution of 3-(4-chloro-phenylamino)-5-(3,5-dimethyl-pyrazol-1-yl) -pyrazine-2-carbaldehyde (80 mg, 0.22 mmol) in methanol (5 mL) and stirred at room temperature for 30 minutes. The reaction was quenched with aqueous sodium hydrogen carbonate and diluted with ethyl acetate. The organic solvents were evaporated and the remaining aqueous phase was extracted with ethyl acetate (3×20 mL). The combined organic phases were washed with brine, dried over sodium sulphate, filtrated and evaporated to give [3-(4-chloro-phenylamino)-5-(3,5-dimethyl-pyrazol-1-yl)-pyrazin-2-yl]-methanol (58 mg, 80%) as the crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415358B2
Source datasetuspto-grants-2013_04
ORD IDord-891c8013effa4b8ea80a01b58cb22095
Source noteuspto-grants-2013_04