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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019697Generated: October 31, 2026

tert-Butyl 4-aminomethyl-4-fluoropiperidine-1-carboxylate → tert-Butyl 4-[(3-ethoxycarbonylisoxazol-5-ylmethoxy-carbonylamino)methyl]-4-fluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/1019697

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-aminomethyl-4-fluoropiperidine-1-carboxylateHCID 40152119—
ReactantEthyl 5-(4-nitrophenoxycarbonyloxymethyl)isoxazole-3-carboxylateHCID 66661006—
Producttert-Butyl 4-[(3-ethoxycarbonylisoxazol-5-ylmethoxy-carbonylamino)methyl]-4-fluoropiperidine-1-carboxylateHCID 6666112325.5%

Reaction Steps

The process is performed according to the procedure described in Example 1 (step 1.6.). Starting with 0.70 g (3.01 mmol) of tert-butyl 4-aminomethyl-4-fluoropiperidine-1-carboxylate (commercial) and 1.11 g (3.31 mmol) of ethyl 5-(4-nitrophenoxycarbonyloxymethyl)isoxazole-3-carboxylate, obtained in step 14.1., 0.33 g of pure product is obtained in the form of an orange-coloured oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716289B2
Source datasetuspto-grants-2014_05
ORD IDord-90508ecd6652446db56b1ffcf62fc5e7
Source noteuspto-grants-2014_05