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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482212Generated: October 30, 2026

Piperidine → (R)-3-(tert-butyldisulfanyl)-2-(methylamino)propanoic acid

https://huagongshe.com/reaction/1482212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantFmoc-N-methyl-S-tert-butylthio-L-cysteineHCID 75409952—
SolventTetrahydrofuranHCID 8028—
Product(R)-3-(tert-butyldisulfanyl)-2-(methylamino)propanoic acidHCID 8966841145.1%

Reaction Steps

Piperidine (1.8 ml, 18.2 mmol) was added to a solution of (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(tert-butyldisulfanyl)propanoic acid (Compound 2c-B) (2.70 g, 6.06 mmol) in tetrahydrofuran (20 ml), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was then concentrated under reduced pressure, and the residue was purified by reverse-phase silica gel column chromatography (10 mM aqueous ammonium acetate solution/methanol=100/0→60/40) to afford (R)-3-(tert-butyldisulfanyl)-2-(methylamino)propanoic acid (Compound 2f-G) (610 mg, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409952B2
Source datasetuspto-grants-2016_08
ORD IDord-188bde7f682d40c5a6d51dc6f665f221
Source noteuspto-grants-2016_08