1-Bromoheptane → HCID 70471697, compound

HRID 745546Notes

Reaction equation

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

Participants

Reactant 2

HCID 123691-Bromoheptane

HCID 54006795HCID 54006795, compound

Product 1

HCID 70471697HCID 70471697, compound

Procedure

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

Sources & evidence

ORD record: ord-a92d7fcef698424fb0860a6e996547d3
Source dataset: uspto-grants-1986_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04599344

Reaction notes

Loading…