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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105434Generated: October 31, 2026

Triphenylphosphine → 4-(1-Oxo-1,2,3,4-tetrahydro-2,4a,5-triaza-fluoren-7-yloxy)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2105434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantDi-tert-butyl diazene-1,2-dicarboxylateHCID 6034084—
Reactant7-hydroxy-3,4-dihydro-2H-2,4a,5-triaza-fluoren-1-oneHCID 68464031—
Product4-(1-Oxo-1,2,3,4-tetrahydro-2,4a,5-triaza-fluoren-7-yloxy)-piperidine-1-carboxylic acid tert-butyl esterHCID 6846472770%

Reaction Steps

The title compound was synthesized in analogy to example 1, from 7-hydroxy-3,4-dihydro-2H-2,4a,5-triaza-fluoren-1-one (example 84, intermediate a)), tert-butyl 4-hydroxy-1-piperidinecarboxylate (commercially available), triphenylphosphine and di-tert-butylazodicarboxylate, to give the desired product as a light brown solid (70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579351B2
Source datasetuspto-grants-2009_08
ORD IDord-40f83609e58346439333069c4fb7dc61
Source noteuspto-grants-2009_08