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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017769Generated: October 30, 2026

Butanoic acid, 4-chloro-, methyl ester → HCID 22897426, compound

https://huagongshe.com/reaction/1017769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanoic acid, 4-chloro-, methyl esterHCID 76612—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22897431HCID 22897431—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetonitrileHCID 6342—
ProductHCID 22897426HCID 22897426—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 65 mg of 1-(S)-(1-(R)-(3,5-bis(trifluoromethyl)-phenyl)ethoxy)-2-(R)-(4-fluorophenyl)-3-(R)-((methylamino)methyl)cyclopentane from Example 18, Step B in 1 mL of acetonitrile was added 0.019 mL of methyl 4-chlorobutyrate and 0.037 mL of DIPEA. The reaction was heated at 50° C. for 48 hours, then an additional 0.038 mL of methyl 4-chlorobutyrate, 0.074 mL of DIPEA and 3 mg of tetrabutylammonium iodide were added and heating continued at 70° C. for 48 hours. The reaction was evaporated under a stream of nitrogen and the residue purified by prep TLC (10% methanol in ethyl acetate) to give 41 mg of title compound and 17 mg of recovered starting material. Mass spec (ESI): 564 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479518B2
Source datasetuspto-grants-2002_11
ORD IDord-409f641db2504f5cb93faa07bf3450bf
Source noteuspto-grants-2002_11