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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458604Generated: October 26, 2026

Cyclohexane, (bromomethyl)- → N-[(1-Cyclohexylmethyl-4-piperidyl)methyl] 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamide

https://huagongshe.com/reaction/1458604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexane, (bromomethyl)-HCID 137636—
ReactantN-(4-Piperidylmethyl) 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamideHCID 9839803—
ProductN-[(1-Cyclohexylmethyl-4-piperidyl)methyl] 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamideHCID 19599430—

Reaction Steps

N-(4-Piperidylmethyl) 3,4-dihydro-2 H-[1,3]oxazino[3,2-a]indole- 10-carboxamide (E21) was alkylated with cyclohexylmethyl bromide using the method of Example 22 with a reaction time of 70 h at room temperature followed by 8 h at reflux temperature. The title compound (E23) was obtained as a white solid (31%) which was converted to its hydrochloride salt and crystallised from acetone/ether as a white solid mp 209°-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852014
Source datasetuspto-grants-1998_12
ORD IDord-88112869bfd541de84420edc79564658
Source noteuspto-grants-1998_12