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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925510Generated: October 31, 2026

Sodium borohydride → HCID 86714222, compound

https://huagongshe.com/reaction/925510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86714221HCID 86714221—
SolventEthanolHCID 702—
ProductHCID 86714222HCID 86714222105.6%

Reaction Steps

Methyl 4-((4-(4-(tert-butoxycarbonyl)piperazin-1-yl)-3-(trifluoromethyl)phenyl)amino)-6-chloro-1,5-naphthyridine-3-carboxylate (0.565 g, 1.0 mmol) was added to ethanol (10 mL), to the system added sodium borohydride (0.228 g, 6 mmol) in batches, stirred at room temperature for 18 h. Ethanol was removed under reduced pressure, added 10 mL of water, and extracted with 80 mL of dichloromethane. The organic layer was dried over anhydrous sodium sulfate, concentrated under reduced pressure to give 0.568 g of a crude solid product. The solid was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284315B2
Source datasetuspto-grants-2016_03
ORD IDord-1d347fa119254d519da5b6e20a0d9daa
Source noteuspto-grants-2016_03