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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176422Generated: November 2, 2026

4-Methoxybutanoyl chloride → tert-Butyl 3-[5-fluoro-2-(4-methoxybutyrylamino)benzyloxy]-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/1176422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybutanoyl chlorideHCID 12794989—
ReactantTert-butyl 3-(2-amino-5-fluorobenzyloxy)-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylateHCID 68499727—
Producttert-Butyl 3-[5-fluoro-2-(4-methoxybutyrylamino)benzyloxy]-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylateHCID 68503209—

Reaction Steps

Analogously to Example 116b, 0.487 g of tert-butyl 3-(2-amino-5-fluorobenzyloxy)-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate and 0.322 g of 4-methoxybutyryl chloride are reacted. The title compound is obtained as a beige oil. Rf=0.22 (1:1 EtOAc-heptane); Rt=5.73.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842688B2
Source datasetuspto-grants-2010_11
ORD IDord-6fbca0a833e34fe39dce7411f5935c7b
Source noteuspto-grants-2010_11