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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748985Generated: October 29, 2026

Morpholine → 3-{4-[4-(2-Tert-butoxycarbonylamino-3-morpholin-4-yl-3-oxo-propyl)-phenoxy]-phenyl}-propionic acid methyl ester

https://huagongshe.com/reaction/748985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant2-Tert-butoxycarbonylamino-3-{4-[4-(2-methoxycarbonyl-ethyl)-phenoxy]-phenyl}-propionic acidHCID 59762802—
SolventDichloromethaneHCID 6344—
Product3-{4-[4-(2-Tert-butoxycarbonylamino-3-morpholin-4-yl-3-oxo-propyl)-phenoxy]-phenyl}-propionic acid methyl esterHCID 5976282074%

Reaction Steps

The compound 4 (2.0 g, 4.6 mmol) was dissolved in CH2Cl2 (25 mL) and stirred at room temperature under an atmosphere of argon. Triethylamine (0.94 mL, 6.76 mmol) and BOP reagent (2.19 g, 4.96 mmol) were added and the reaction mixture was stirred for 15 min. Morpholine (0.79 mL, 9.02 mmol) was added and the resulting solution was stirred at room temperature for about 1 h. The solvent was removed under reduced pressure and the resulting oil was taken up in EtOAc (60 mL). The organic layer was extracted with 1.0 N NaOH (1×10 mL), water (2×20 mL) and brine (1×20 mL). Drying and concentration of the organic layer gave the desired amide 13 (1.7 g, ˜74%). 1H NMR (400 MHz, DMSO-d6): 7.24 (d, J=8.8 Hz, 2H), 7.20 (d, J=8.4 Hz, 2H), 7.17 (d, J=8.4 Hz, 2H), 6.90 (d, J=8.4 Hz, 2H), 6.86 (d, J=8.4 Hz, 2H), 4.56 (m, 1H), 3.58 (s, 3H), 3.24-3.54 (m, 8H), 2.74-2.87 (m, 4H), 2.62 (t, J=6.0 Hz, 2H), 1.32 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399786B2
Source datasetuspto-grants-2008_07
ORD IDord-abf18beb9afc40ce82967314aa3264a2
Source noteuspto-grants-2008_07