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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222702Generated: October 29, 2026

Piperidine → HCID 10248610, compound

https://huagongshe.com/reaction/222702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 57440293HCID 57440293—
SolventDichloromethaneHCID 6344—
ProductHCID 10248610HCID 10248610—

Reaction Steps

Piperidine (0.1 ml, 1.1 mmol) was added to a stirred solution of 3-cyclobutyl-7-{[4-(1H-imidazol-1-yl)-4-oxobutyl]oxy}-2,3,4,5-tetrahydro-1H-3-benzazepine (E167, Step 1) (150 mg, 0.42 mmol) in dichloromethane (5 ml). After stirring at room temperature for 5 days the reaction mixture was concentrated in vacuo and the resulting residue was purified by column chromatography eluting with a mixture of 0.880 ammonia:ethanol:dichloromethane (1:9:90) to afford the title compound (E167); MS (ES+) m/e 371 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207331B2
Source datasetuspto-grants-2012_06
ORD IDord-53e185bc2c2d45a8aed0c57767fb97a9
Source noteuspto-grants-2012_06