1-Bromoheptane → HCID 23313715, compound

HRID 745554Notes

Reaction equation

[N:1]12[CH2:8][CH2:7][CH:4]([CH2:5][CH2:6]1)[CH2:3][CH:2]2[CH2:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][C:15]([NH:18][S:19]([CH3:22])(=[O:21])=[O:20])=[CH:14][CH:13]=1.[CH2:23]([Br:30])[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]>>[Br-:30].[CH2:23]([N+:1]12[CH2:8][CH2:7][CH:4]([CH2:5][CH2:6]1)[CH2:3][CH:2]2[CH2:9][CH2:10][CH2:11][C:12]1[CH:13]=[CH:14][C:15]([NH:18][S:19]([CH3:22])(=[O:20])=[O:21])=[CH:16][CH:17]=1)[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]

Participants

Reactant 2

HCID 123691-Bromoheptane

HCID 23313723HCID 23313723, compound

Product 1

HCID 23313715HCID 23313715, compound

Procedure

React N-[4-(3-(1-azabicyclo[2.2.2]oct-2-yl)propyl)phenyl]methanesulfonamide with heptyl bromide in a manner similar to Example II, Method A, to afford the title compound.

Sources & evidence

ORD record: ord-030009230a504f739a705af658a3331f
Source dataset: uspto-grants-1986_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04599344

Reaction notes

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