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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635050Generated: November 2, 2026

Ammonia → 4-Piperidinylmethyl 4-amino-5-chloro-2-methoxybenzoate

https://huagongshe.com/reaction/1635050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1,1-Dimethylethyl 4-[[(4-amino-5-chloro-2-methoxy-benzoyl)oxy]methyl]-1-piperidine-carboxylateHCID 22662761—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
Product4-Piperidinylmethyl 4-amino-5-chloro-2-methoxybenzoateHCID 2266275765%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of intermediate 10 (18 g) in HCl (25 ml) and THF (250 ml) was stirred for 30 minutes at 70° C. The reaction mixture was cooled, alkalized with aqueous ammonia and the layers were separated. The aqueous layer was extracted twice with THF. The combined organic layers were dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/(CH3OH/NH3) 90/10). The pure fractions were collected and the solvent was evaporated. The residue (10 g) was dissolved in CHCl3, washed with aqueous ammonia, dried, filtered and the solvent was evaporated. The residue was suspended in DIPE, filtered off and dried, yielding 8.5 g (65%) 4-piperidinylmethyl 4-amino-5-chloro-2-methoxybenzoate (intermediate 11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509339B2
Source datasetuspto-grants-2003_01
ORD IDord-207495cabc0d447eb954f1e5c3bcc3ef
Source noteuspto-grants-2003_01