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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707137Generated: October 29, 2026

Sodium borohydride → Trifluoroacetic acid

https://huagongshe.com/reaction/707137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86636772HCID 86636772—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductTrifluoroacetic acidHCID 6422—
ProductHCID 44548946HCID 44548946—

Reaction Steps

1-(4-(4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-(4-oxopiperidin-1-yl)-1,3,5-triazin-2-yl)phenyl)-3-(pyridin-4-yl)urea-TFA (56 mg) was taken up in methanol/tetrahydrofuran (1:1, 6 mL), and the mixture at 0° C. was treated with sodium borohydride (10 mg). After warming to room temperature, the mixture was concentrated to a residue which then was purified by HPLC to give the title compound as its TFA salt.; MS (ES+) 503.0 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174963B2
Source datasetuspto-grants-2015_11
ORD IDord-d61331c0ec554042a9876663fde55c67
Source noteuspto-grants-2015_11