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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430648Generated: November 2, 2026

4-Methylmorpholine → HCID 59363835, compound

https://huagongshe.com/reaction/1430648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 59363828HCID 59363828—
ReactantHCID 72221007HCID 72221007—
SolventDichloromethaneHCID 6344—
ProductHCID 59363835HCID 59363835250.2%

Reaction Steps

To a mixture of 2-(2,4-Difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionic acid (0.110 g, 0.22 mmol), (2-Amino-5-chloro-thiazol-4-yl)-acetic acid methyl ester (0.071 g, 0.32 mmol), HOBt (0.052 g, 0.38 mmol), and EDCI (0.074 g, 0.38 mmol) in methylene dichloride (10 ml) was added N-methylmorpholine (0.039 g, 0.38 mmol). The resulting mixture was stirred at room temperature for overnight followed by dilution with 10 ml methylene dichloride. The reaction mixture was poured onto water (20 ml), and organic layer separated, washed with water (2×20 ml), brine (20 ml), dried over sodium sulfate and solvent evaporated to get residue which was purified by preparative TLC using 50% ethyl acetate in hexane as mobile. To give desired compound (0.30 g). 1H NMR (400 MHz, CDCl3): δ 1.45 (t, J=7.2 Hz, 3H), 1.93 (s, 3H), 3.14 (s, 3H), 3.77 (d, J=2.8 Hz, 1H), 4.26 (q, J=7.2 Hz, 1H), 6.69-6.77 (m, 2H), 6.96-7.02 (m, 1H), 7.89 (d, J=8.4 Hz, 2H), 8.07 (d, J=8.4 Hz, 1H); MS (D) m/z: 559.00 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940900B2
Source datasetuspto-grants-2015_01
ORD IDord-0171cb11de6e40a3b880320a3a0f223e
Source noteuspto-grants-2015_01