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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274599Generated: October 30, 2026

2-Methyl-2-butene → 1-Ethyl-3-propyl-4-[[2'-[[(trifluoromethyl)sulphonyl]amino][1,1'-biphenyl]-4-yl]methyl]-1H-pyrazole-5-carboxylic acid

https://huagongshe.com/reaction/274599

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantN-[4'-[[1-Ethyl-5-formyl-3-propyl-1H-pyrazol-4-yl]methyl][1,1'-biphenyl]-2-yl]trifluoromethanesulphonamideHCID 20093388—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
Product1-Ethyl-3-propyl-4-[[2'-[[(trifluoromethyl)sulphonyl]amino][1,1'-biphenyl]-4-yl]methyl]-1H-pyrazole-5-carboxylic acidHCID 2009331556.3%

Reaction Steps

A solution of sodium chlorite (0.4 g) and sodium dihydrogen orthophosphate (2.56 g) in water (5 ml) was added to a solution of the product of Example 88 (430 mg) and 2-methyl-2-butene (4.5 ml, 2M solution in THF) in t-butanol (5 ml) and THF (10 ml) and the resulting mixture stirred for 3 h. Solvent was removed in vacuo, the residue taken up in dichloromethane (10 ml) and washed with water (10 ml). 2N Sodium hydroxide (10 ml) was added to the organic solution and the organic layer removed. 2N Hydrochloric acid (~11 ml) was added to the aqueous phase which was then extracted with ethyl acetate (2×15 ml). The dried organic extracts were evaporated in vacuo to give a yellow gummy solid which was recrystaltised from System D (1:1) to give the title compound as a white solid (250 mg) m.p. 68°-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389659
Source datasetuspto-grants-1995_02
ORD IDord-832daeb6959749d0885e9f6450ad82d3
Source noteuspto-grants-1995_02