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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371449Generated: October 29, 2026

Diisopropylethylamine → N-{[(2S)-4-(2,3-dichlorobenzyl)morpholin-2-yl]methyl}-N'-prop-2-ynylurea

https://huagongshe.com/reaction/1371449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Nitrophenyl prop-2-ynylcarbamateHCID 23089179—
Reactant[(2S)-4-(2,3-dichlorobenzyl)morpholin-2-yl]methylamineHCID 68884489—
SolventDichloromethaneHCID 6344—
ProductN-{[(2S)-4-(2,3-dichlorobenzyl)morpholin-2-yl]methyl}-N'-prop-2-ynylureaHCID 8676034651.5%

Reaction Steps

A solution of Intermediate 22 (0.024 g) in dichloromethane (1 ml) was stirred with Intermediate 20 (0.033 g) and N,N-diisopropylethylamine (0.022 ml) for 3 h at 23° C. The solvent was removed in vacuo and the residue was purified by solid phase extraction (Isolute SCX sulphonic acid column) eluting with methanol followed by 10% 0.880 ammonia solution in methanol. The basic fraction was concentrated in vacuo, and the residue was dissolved in dichloromethane (5 ml), and the solution shaken with polystyrene methyl isocyanate resin (Argonaut technologies, 0.256 g, 1.43 mmol/g) for 16 h. The solution Was drained from the resin and the resin washed with dichloromethane (8 ml); the combined filtrate and washings were concentrated in vacuo to give the title compound as a pale yellow gum (0.02 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157457B2
Source datasetuspto-grants-2007_01
ORD IDord-e36ede6d838840ebaf43c9322f13bf2c
Source noteuspto-grants-2007_01