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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844590Generated: October 26, 2026

Diisopropylethylamine → HCID 67217548, compound

https://huagongshe.com/reaction/1844590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantN-(3-amino-5-tert-butyl-2-methoxyphenyl)methanesulphonamide-hydrochlorideHCID 21079205—
Reactant3-(Benzyloxy)-4-methylbenzoic acidHCID 22903188—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 67217548HCID 67217548—

Reaction Conditions

Temperature50 °C

Reaction Steps

10.59 g of O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyl-uronium hexafluorophosphate, 9.54 ml diisopropylethylamine and 1.26 g 1-hydroxy-7-azabenzotriazole are added to 4.50 g 3-benzyloxy-4-methyl-benzoic acid in 25 ml N,N-dimethylformamide under an argon atmosphere. The mixture is stirred for 15 minutes at ambient temperature, before 5.74 g N-(3-amino-5-tert-butyl-2-methoxyphenyl)methanesulphonamide-hydrochloride are added. The reaction mixture is stirred overnight at 50° C. After cooling to ambient temperature the reaction mixture is diluted with ethyl acetate, washed with water, 1 N hydrochloric acid and saturated aqueous sodium chloride solution, dried on magnesium sulphate and evaporated down. The flask residue is stirred with methanol, and the resulting white precipitate is suction filtered and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946438B2
Source datasetuspto-grants-2015_02
ORD IDord-0ef8f2f3e5bb4b97af5414d0a35b9125
Source noteuspto-grants-2015_02