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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910482Generated: October 28, 2026

Triethylamine → HCID 44155146, compound

https://huagongshe.com/reaction/910482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl carbazateHCID 70091—
Reactant1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
ReactantHCID 67389861HCID 67389861—
SolventDichloromethaneHCID 6344—
ProductHCID 44155146HCID 44155146—

Reaction Steps

A solution of 1.0 mmol of [(2R,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-1-(toluene-4-sulfonyl) -piperidin-2-yl]-acetic acid (example 1g) in 5 ml of CH2Cl2 is treated at RT with 1.5 mmol of 1-chloro-N,N,2-trimethylpropenylamine, and stirred at RT for 2.5 h. This solution is added slowly, at 0° C., to a solution of 5 mmol of tert-butyl carbazate [870-46-2] and 5 mmol of Et3N in 1 ml of CH2Cl2. The reaction mixture is stirred at 4° C. for 16.5 h, then quenched with H2O. The aqueous layer is extracted with CH2Cl2 (2×). The combined organic extracts are washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The residue is purified by flash chromatography (SiO2 60 F) to afford the title compound, which is identified based on its Rf value.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022069B2
Source datasetuspto-grants-2011_09
ORD IDord-deae28143208489f9ee738af94aab6b1
Source noteuspto-grants-2011_09