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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017981Generated: November 1, 2026

Diisopropylethylamine → HCID 178424382, compound

https://huagongshe.com/reaction/1017981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-((((2-Methylphenyl)amino)carbonyl)amino)benzeneacetic acidHCID 6605254—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 18404651HCID 18404651—
SolventDimethylformamideHCID 6228—
ProductHCID 178424382HCID 178424382—

Reaction Steps

A mixture of 5-amino-(pyrid-2-yl)-thioacetic acid methyl ester [930 mg, Reference Example 1(a)], 4-[3-(2-methylphenyl)ureido]phenylacetic acid (1.26 g, prepared as described in Example 21 of International Patent Application Publication No. WO 96/22966), O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (1.69 g) and diisopropylethylamine (1.2 g) in dimethylformamide (50 ml) was stirred at ambient temperature for 1 hour. The mixture was evaporated then poured into water (500 ml). The resultant solid was washed with water (50 ml) and then washed twice with diethyl ether (50 ml). The solid was suspended in methanol (100 ml), then treated with sodium hydroxide solution (10 ml, 1M). The mixture was heated at reflux for 5 hours, then cooled, then evaporated. The residue was treated with hydrochloric acid (200 ml, 1M). The resultant solid was filtered, washed with water (20 ml), then washed twice with diethyl ether (20 ml), then recrystallised from ethanol to give the title compound (220 mg) as a yellow solid, m.p. >235° C. (with decomposition). MS: MH+ 451.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479519B1
Source datasetuspto-grants-2002_11
ORD IDord-2a7232f88efd403fa20b4f00d081bb9d
Source noteuspto-grants-2002_11