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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268742Generated: November 1, 2026

N-benzyl-N-ethylethanamine;1,4-bis(ethenyl)benzene;styrene → N-{2-Chloro-4-[(1-isopropyl-4-piperidinyl)oxy]benzoyl}-5-fluoro-isoindoline hydrochloride

https://huagongshe.com/reaction/268742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-benzyl-N-ethylethanamine;1,4-bis(ethenyl)benzene;styreneHCID 16212021—
Reactant5-fluoro-2,3-dihydro-1H-isoindole hydrochlorideHCID 17986286—
Reactant2-Chloro-4-[(1-isopropyl-4-piperidinyl)oxy]benzoyl chloride hydrochlorideHCID 17986295—
SolventDichloromethaneHCID 6344—
ProductN-{2-Chloro-4-[(1-isopropyl-4-piperidinyl)oxy]benzoyl}-5-fluoro-isoindoline hydrochlorideHCID 1798627770%

Reaction Steps

A stirred mixture of 2-chloro-4-[(1-isopropyl-4-piperidinyl)oxy]benzoyl chloride hydrochloride (D33) (0.20 g) and diethylaminomethyl polystyrene (3.2 mmol/g, 1.0 g) in DCM (10 ml) at rt was treated with 5-fluoroisoindoline hydrochloride (D8) (0.10 g) and stirred for 16 h. The reaction mixture was chromatographed directly [silica gel, step gradient 0-10% MeOH (containing 10% 0.880 ammonia solution) in DCM]. Fractions containing the required product were evaporated, redissolved in DCM, treated with excess hydrogen chloride (1M solution in diethyl ether) and then concentrated. The residue was crystallised from acetone to yield the title compound (E63) as a white solid (0.09 g). MS electrospray (+ion) 417/419 (MH+). 1H NMR δ (DMSO-d6): 9.80 (1H, s), 7.22-6.81 (6H, m), 4.70-4.39 (3H, m), 4.25 (3H, m), 3.24 (2H, m), 2.88 (2H, m), 2.10-1.70 (4H, m), 1.06 (6H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446103B2
Source datasetuspto-grants-2008_11
ORD IDord-929a51ba2232440f937c281627b27007
Source noteuspto-grants-2008_11