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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063218Generated: November 2, 2026

Morpholine → HCID 69736315, compound

https://huagongshe.com/reaction/1063218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(S)-(-)-N-Boc-prolinolHCID 643448—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 69736315HCID 6973631540%

Reaction Conditions

Temperature110 °C

Reaction Steps

Methanesulfonyl chloride (1.7 g, 14.9 mmol) was added dropwise to a solution of (S)-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (1.5 g, 7.45 mmol) and triethylamine (753 mg mg, 7.45 mmol) in CH2Cl2 at 0° C. After 3 h reaction mixture was concentrated to give a white solid. The resulting solid was suspended in toluene, morpholine (1.3 g, 14.9 mmol) was added, and the resulting mixture was heated to 110° C. in a sealed tube. After 12 h the reaction mixture was concentrated, the resulting residue was dissolved in EtOAc and water, the layers were separated, and the aqueous was further extracted with EtOAc. The combined organic extracts were dried over Na2SO4, and the material was purified on silica gel by flash column chromatography CH2Cl2/MeOH/NH4OH (98.5/1/0.5) to afford the title compound as a white solid (800 mg, 40%). MS: 271.2 (MH+); HPLC Rf: n.d.; HPLC purity: n.d.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964961B2
Source datasetuspto-grants-2005_11
ORD IDord-867fd983e98547dc9f62cf8691769a0d
Source noteuspto-grants-2005_11