Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403281Generated: October 31, 2026

Sodium Chloride → HCID 68325408, compound

https://huagongshe.com/reaction/2403281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68325428HCID 68325428—
SolventDimethylformamideHCID 6228—
ProductHCID 68325408HCID 6832540879%

Reaction Steps

To a stirred solution of (S)-2-[4-(4-chloro-phenylamino)-phenyl]-morpholine-4-carboxylic acid tert-butyl ester (60 mg) in DMF (2 ml) was added sodium hydride (6.2 mg) and stirring was continued at room temperature for 15 min. Iodomethane (24.3 mg) was then added dropwise. The reaction mixture was stirred at room temperature for 1 h. TLC at t=1 h showed the reaction was incomplete with some starting material remaining A second portion of sodium hydride (6.2 mg) was added. After stirring at room temperature for 15 min, iodomethane (24.3 mg) was added. Stirring was continued for a further hour. TLC then showed the reaction was complete. The reaction mixture was poured into sat. aq. NaCl and extracted twice with EtOAc. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The crude material was purified by flash column chromatography (silica gel; gradient: 0% to 50% EtOAc in heptane) to afford (S)-2-{4-[(4-chloro-phenyl)-methyl-amino]-phenyl}-morpholine-4-carboxylic acid tert-butyl ester (49 mg, 79%) as a colourless gum. MS (ISP): 405.4 ([{37Cl}M+H]+), 403.4 ([{35Cl}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802673B2
Source datasetuspto-grants-2014_08
ORD IDord-c158e4134fcb40ab989a157a6deb5cbe
Source noteuspto-grants-2014_08