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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049379Generated: November 2, 2026

HCID 90403394, compound → HCID 178433219, compound

https://huagongshe.com/reaction/1049379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 90403394HCID 90403394—
SolventMethanolHCID 887—
ProductHCID 178433219HCID 17843321950%

Reaction Steps

A solution of (4-(4-((2-Methyl-6-(3-pivaloylureido)pyridin-3-yl)oxy)pyridin-2-yl)-1H-1,2,3-triazol-1-yl)methyl pivalate (0.16 g, 0.314 mmol) and TEA (0.175 mL, 1.256 mmol) in MeOH (5 mL) was stirred at 40° C. for ˜40 h. The solvent was evaporated to dryness and the residue was purified by silica gel chromatography (MeOH/DCM), and lyophilized from MeCN/H2O to afford N-((5-((2-(1H-1,2,3-triazol-4-yl)pyridin-4-yl)oxy)-6-methylpyridin-2-yl)carbamoyl)pivalamide (62 mg, 50%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 11.18 (s, 1H), 10.40 (br s, 1H), 8.49 (d, J=5.9 Hz, 1H), 8.23 (br s, 1H), 7.93 (br s, 1H), 7.70 (d, J=8.8 Hz, 1H), 7.35 (br s, 1H), 6.90 (d, J=5.5 Hz, 1H), 2.26 (s, 3H), 1.21 (s, 9H); MS (ESI) m/z: 396.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382228B2
Source datasetuspto-grants-2016_07
ORD IDord-3fec5dd690fd4dab8b1ef046285885e5
Source noteuspto-grants-2016_07