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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811731Generated: October 26, 2026

Piperidine → ((S)-3-amino-4-morpholin-4-yl-4-oxobutyl)carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1811731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant[(S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-morpholin-4-yl-4-oxobutyl]carbamic acid tert-butyl esterHCID 59224644—
SolventDimethylformamideHCID 6228—
Product((S)-3-amino-4-morpholin-4-yl-4-oxobutyl)carbamic acid tert-butyl esterHCID 592246970.1%

Reaction Steps

[(S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-morpholin-4-yl-4-oxobutyl]carbamic acid tert-butyl ester (172 mg, 0.338 mol) obtained in Step 1 above was dissolved in N,N-dimethylformamide (1.5 ml), and then piperidine (84 μl) was added thereto. After the solution was stirred at room temperature for 30 minutes, the solvent was concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (developing solvent: dichloromethane:methanol=20:1) to yield ((S)-3-amino-4-morpholin-4-yl-4-oxobutyl)carbamic acid tert-butyl ester (95 mg) as a colorless oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362236B2
Source datasetuspto-grants-2013_01
ORD IDord-bccbfa6db8b7442b8e1cf2c3aa43114d
Source noteuspto-grants-2013_01