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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775887Generated: November 3, 2026

Piperidine → HCID 117748920, compound

https://huagongshe.com/reaction/1775887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 117748919HCID 117748919—
SolventDichloromethaneHCID 6344—
ProductHCID 117748920HCID 117748920233.2%

Reaction Steps

To a stirring solution of tert-butyl (R)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylamino)-4-oxobutanoate (226 mg, 0.53 mmol), in DCM (1.05 mL) was added piperidine (263 μL, 2.7 mmol). The reaction mixture was stirred for 1 h at room temperature. The solvent was evaporated to afford 250 mg (100%) of tert-butyl (R)-3-amino-4-(methylamino)-4-oxobutanoate as a mixture with 1-((9H-fluoren-9-yl)methyl)piperidine. The mixture was used without purification in the next reaction. LCMS-ESI (m/z) calculated for C9H18N2O3: 202.1. found 225.1 [M+Na]+, tR=0.50 min. (Method 15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260427B2
Source datasetuspto-grants-2016_02
ORD IDord-5263dfa624de465e9595e6a3092cb7ac
Source noteuspto-grants-2016_02