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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275890Generated: October 31, 2026

Diisopropylethylamine → HCID 57162964, compound

https://huagongshe.com/reaction/275890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactantethyl N-(3,4-dimethoxybenzyl)-beta-alaninateHCID 1908440—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 54377278HCID 54377278—
SolventDimethylformamideHCID 6228—
ProductHCID 57162964HCID 5716296487.1%

Reaction Steps

A solution of ({[3-methoxy-4-(3-o-tolylureido)phenyl]-acetyl}-N-methylamino)-acetic acid [18.4 g, Reference Example 1] and 3-(3,4-dimethoxy-benzylamino)-propionic acid ethyl ester [13.4 g, Reference Example 2(a)] in dimethylformamide (400 ml) was treated with [O-(7-azabenzotriazol-1-yl)-1,1,3,3,-tetramethyluronium hexafluorophosphate] (19.1 g) and diisopropylethylamine (10.5 ml). After stirring at ambient temperature for 20 hours the reaction mixture was evaporated to dryness. The residue was treated with water (800 ml) followed by hydrochloric acid (175 ml 1 M) and the mixture was extracted twice with ethyl acetate (500 ml). The combined organic extracts were washed with hydrochloric acid (500 ml, 1M), then with water (400 ml), then with saturated aqueous sodium bicarbonate solution (500 ml), then dried over magnesium sulphate and then evaporated. The residual oil was subjected to flash chromatography on silica eluting with a mixture of dichloromethane and methanol (49:1, v/v) to give the title compound as a fawn coloured foam (26.4 g), m.p. 97-105° C. [Elemental analysis:- C,63.4; H,6.7; N,8.7% Calculated for C34H42N4O8.0.5H2O:- C,63.3; H,6.8; N,8.8%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352977B1
Source datasetuspto-grants-2002_03
ORD IDord-ce5889029f4842719729a7d92be8298d
Source noteuspto-grants-2002_03