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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268740Generated: October 31, 2026

Isoindoline → HCID 17986321, compound

https://huagongshe.com/reaction/268740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoindolineHCID 422478—
ReactantN-benzyl-N-ethylethanamine;1,4-bis(ethenyl)benzene;styreneHCID 16212021—
ReactantHCID 17986293HCID 17986293—
SolventDichloromethaneHCID 6344—
ProductHCID 17986321HCID 17986321134.5%

Reaction Steps

A stirred mixture of 2-chloro-4-(3-piperidin-1-ylpropoxy)benzoyl chloride hydrochloride (D28) (0.10 g) and diethylaminomethyl polystyrene (3.2 mmol/g, 0.8 g) in DCM (10 ml) at rt was treated with isoindoline (0.031 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 (E61) as a white solid (0.083 g). MS electrospray (+ion) 399/401 (MH+). 1H NMR δ (DMSO-d6): 9.90 (1H, s), 7.41 (2H, m), 7.28 (3H, m), 7.11 (1H, s), 7.02 (1H, m), 4.83 (2H, s), 4.50 (2H, s), 4.14 (2H, t, J=5.9 Hz), 3.45 (2H, m), 3.25 (2H, m), 2.90 (2H, m), 2.18 (2H, m), 1.87-1.30 (6H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446103B2
Source datasetuspto-grants-2008_11
ORD IDord-1bd3a5b18183442e976ee3a8d8d82c0e
Source noteuspto-grants-2008_11