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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269651Generated: October 30, 2026

Piperidine → tert-butyl[(1S)-4-[(tert-butoxycarbonyl)amino]-1-({[(2s)-2,5-diamino-5-oxopentanoyl]amino}methyl)butyl]carbamate

https://huagongshe.com/reaction/269651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant9h-fluoren-9-ylmethyl{(1S)-4-amino-1-[({(2s)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)carbonyl]-4-oxobutyl}carbamateHCID 70806689—
SolventDimethylformamideHCID 6228—
Producttert-butyl[(1S)-4-[(tert-butoxycarbonyl)amino]-1-({[(2s)-2,5-diamino-5-oxopentanoyl]amino}methyl)butyl]carbamateHCID 88986898—

Reaction Steps

A solution of 33 mg (0.05 mmol) of 9H-fluoren-9-ylmethyl{(1S)-4-amino-1-[({(2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)carbonyl]-4-oxobutyl}carbamate (Example 129A) in 1 ml of dimethylformamide is stirred after the addition of 4 mg (0.05 mmol) of piperidine at room temperature for 45 min. The solvent is evaporated and the crude product is reacted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446102B2
Source datasetuspto-grants-2008_11
ORD IDord-3c17c462b843499a943ae187e63c644a
Source noteuspto-grants-2008_11