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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372843Generated: October 30, 2026

HCID 131717218, compound → HCID 178441615, compound

https://huagongshe.com/reaction/2372843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131717218HCID 131717218—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178441615HCID 178441615—

Reaction Steps

A solution of 2-n-butyl-3-[(2'-(N-triphenylmethyl-tetrazol-5-yl)-biphen-4-yl)-methyl]-5-ethyl-6-methylpyrimidin-4(3H)-one (from Example 5) in 4 mL acetic acid and 2 mL water was stirred at room temperature for 6 hours. The reaction mixture was diluted with brine and extracted three times with ether. The combined organic material was washed with brine, was dried over MgSO4, was stripped of solvent in vacuo, and then was MPLC'd in 1 acetic acid/39 hexane/60 ethyl acetate to give the title compound as a white foam. 1H NMR (300 MHz, CDCl3) δ7.87 (m, 1H), 7.58 (m, 1H), 7.49 (m, 1H), 7.40 (m, 1H), 7.02 (4 line m, 4H), 5.19 (br s, 2H), 2.57 (3 line m, 2H), 2.42 (4 line m, 2H), 2.24 (s, 3H), 1.63 (m, 2H), 1.34 (m, 2H), 0.96 (3 line m, 3H), 0.88 (3 line m, 3H); IR (CHCl3) 3420 (br), 3020, 1645, 1530, 1120 cm-1 ; FABMS: 429 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100897
Source datasetuspto-grants-1992_03
ORD IDord-1cf66c2a8576479eb16e7f1daf0a88b9
Source noteuspto-grants-1992_03