HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268738Generated: October 31, 2026
Isoindoline → N-{4-[(1-Cyclobutyl-4-piperidinyl)oxy]benzoyl}isoindoline hydrochloride
https://huagongshe.com/reaction/268738
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoindoline | HCID 422478 | — |
| Reactant | N-benzyl-N-ethylethanamine;1,4-bis(ethenyl)benzene;styrene | HCID 16212021 | — |
| Reactant | 4-[(1-Cyclobutyl-4-piperidinyl)oxy]benzoyl chloride hydrochloride | HCID 17986264 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{4-[(1-Cyclobutyl-4-piperidinyl)oxy]benzoyl}isoindoline hydrochloride | HCID 17986299 | 70.4% |
Reaction Steps
A stirred mixture of 4-[(1-cyclobutyl-4-piperidinyl)oxy]benzoyl chloride hydrochloride (D25) (0.25 g) and diethylaminomethyl polystyrene (3.2 mmol/g, 1.13 g) in DCM (10 ml) at rt was treated with isoindoline (0.098 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 (E59) as a white powder (220 mg). MS electrospray (+ion) 377 (MH+). 1H NMR δ (DMSO-d6): 10.62 (1H, s), 7.62 (2H, m), 7.40-7.25 (4H, m), 7.08 (2H, m) 4.82 (4H, m), 4.64 (1H, m), 3.81-3.58. (1H, m), 3.45-3.20 (2H, m), 2.95 (2H, m), 2.38-1.62 (10H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07446103B2 |
|---|
| Source dataset | uspto-grants-2008_11 |
|---|
| ORD ID | ord-7fbf65022b4d4ef0acc5a2c28b6088e8 |
|---|
| Source note | uspto-grants-2008_11 |
|---|