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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375085Generated: November 2, 2026

Diisopropylethylamine → HCID 69419383, compound

https://huagongshe.com/reaction/1375085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-Methoxy-4-o-tolylureidophenylacetic acidHCID 11449840—
Reactant[2-(4-Amino-phenyl)-indan-2-yl]-acetic Acid Ethyl EsterHCID 69419599—
SolventDimethylformamideHCID 6228—
ProductHCID 69419383HCID 6941938319%

Reaction Steps

A solution of [2-(4-amino-phenyl)-indan-2-yl]-acetic acid ethyl ester (0.158 g, Reference Example 10) in dimethylformamide (2 mL) was treated with a solution of [3-methoxy-4-(3-o-tolyl-ureido)-phenyl]-acetic acid (0.169 g) in dimethylformamide (2 mL) which had been treated with diisopropylethylamine (1.3 mL) and a solution of O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (0.223 g) in dimethylformamide (2 mL). After stirring at room temperature for 2 hours the reaction mixture was evaporated and the residue was partitioned between ethyl acetate (30 mL) and hydrochloric acid (30 mL, 0.5N). The organic phase was washed with hydrochloric acid (30 mL, 0.5N), then with saturated sodium hydrogen carbonate solution (30 mL), then dried over magnesium sulfate and then evaporated. The residual beige coloured solid was subjected to chromatography on silica eluting with a mixture of ethyl acetate and cyclohexane (2:1, v/v) to give the title compound (0.06 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166616B2
Source datasetuspto-grants-2007_01
ORD IDord-b0119a1b56204874adefe6de50e8ead5
Source noteuspto-grants-2007_01