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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063650Generated: November 2, 2026

Ethylmorpholine → HCID 178484646, compound

https://huagongshe.com/reaction/1063650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
Reactant2-(Methylamino)ethanolHCID 8016—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 178483642HCID 178483642—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
ProductHCID 178484646HCID 17848464698%

Reaction Steps

To a solution of 200 mg (0.67 mmol) of trans-{4-[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-cyclohexyl}-acetic acid and 0.065 mL (0.8 mmol, 1.2 eq) of 2-(methylamino)-ethanol were added 0.4 mL (3.3 mmol, 5 eq) of 4-ethylmorpholine and 0.31 g (0.7 mmol, 1.05 eq) of BOP at RT. The solution was stirred at RT for 3 h, diluted with ether and 1M HCl was added. The phases were separated and the organic phases were washed with water and brine and dried over magnesium sulfate. Evaporation yielded 234 mg (quantitative) of crude trans [2-(4-{[(2-hydroxy-ethyl)-methyl-carbamoyl]-methyl}-cyclohexyl)-ethyl]-methyl-carbamic acid tert-butyl ester as colorless oil, MS: 357 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06965048B2
Source datasetuspto-grants-2005_11
ORD IDord-a494250514804024845024f33e62e5ec
Source noteuspto-grants-2005_11