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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524438Generated: October 31, 2026

Sodium borohydride → HCID 86669560, compound

https://huagongshe.com/reaction/524438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86669561HCID 86669561—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 86669560HCID 8666956056.1%

Reaction Steps

To a stirred solution of 2-(4-Cyclopropanesulfonyl-phenyl)-N-[5-(4-formyl-phenoxy)-thiazol-2-yl]-2-(tetrahydro-pyran-4-yloxy)-acetamide (Example A74; 0.2 g, 0.36 mmol) in 10 mL methanol, sodium borohydride (0.027 g, 0.73 mmol) was added in portions at 0° C. After complete addition reaction mixture was stirred for 1 hr at 0° C. to 10° C. Completion of the reaction was confirmed by TLC, then methanol was evaporated on rotavapour. Reaction mixture was diluted with ethyl acetate (3×20 mL), organic layer was washed with water and brine, dried (Na2SO4) and concentrated in vacuo. Purified by PREP TLC to afford title compound (0.110 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340506B2
Source datasetuspto-grants-2016_05
ORD IDord-71859b693dd8428f8f239bf3e0d6edfc
Source noteuspto-grants-2016_05