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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611598Generated: November 1, 2026

Tetrahydrofuran → HCID 53771767, compound

https://huagongshe.com/reaction/611598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Chloro-4,6-dimethoxy-1,3,5-triazineHCID 18450—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
Reactant1-((Tert-butoxy)carbonyl)piperidine-3-carboxylic acidHCID 2735647—
SolventEthyl AcetateHCID 8857—
ProductHCID 53771767HCID 5377176793.9%

Reaction Steps

4.59 g of (RS)-piperidine-1,3-dicarboxylic acid 1-tert.-butyl ester, 3.51 g of 2-chloro4,6-dimethoxy-[1,3,5]-triazine (CDMT), 60 ml of THF and 2.25 ml of N-MM are stirred under argon at 0° C. for 3 hrs. After the addition of 3.07 g of β-alanine ethyl ester hydrochloride and 2.25 ml of N-MM the mixture is stirred at RT for 18 hrs. The reaction mixture is diluted with ethyl acetate and washed in sequence with ice-cold dilute hydrochloric acid, water, dilute sodium carbonate solution, water and saturated sodium chloride solution. After drying over sodium sulphate and evaporation of the solvent there are obtained 6.16 g of (RS)-3-(2-ethoxycarbonyl-ethylcarbamoyl)-piperidine-1-carboxylic acid tert.-butyl ester as a pale yellow oil. MS: 329 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06001855
Source datasetuspto-grants-1999_12
ORD IDord-f05e365207ce4b0e9cadb6b65e45f4c5
Source noteuspto-grants-1999_12