Iodoethane → HCID 22647204, compound

HRID 394043Notes

Reaction equation

[CH:1]1([CH2:9][N:10]2[CH2:15][CH2:14][CH2:13][CH:12]([CH2:16][NH:17][C:18](=[O:47])[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][NH:24][C:25](=[O:46])[CH2:26][C:27]([C:40]3[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=3)([C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)[C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[CH2:11]2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:48]([I:50])[CH3:49]>>[I-:50].[CH:1]1([CH2:9][N+:10]2([CH2:48][CH3:49])[CH2:15][CH2:14][CH2:13][CH:12]([CH2:16][NH:17][C:18](=[O:47])[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][NH:24][C:25](=[O:46])[CH2:26][C:27]([C:34]3[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=3)([C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=3)[C:40]3[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=3)[CH2:11]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]1

Participants

Reactant 2

HCID 6340Iodoethane

HCID 12149953HCID 12149953, compound

Product 1

HCID 22647204HCID 22647204, compound

Procedure

The title compound was prepared by a method similar to Example 130, using N-(6-{(1-cyclooctylmethyl-3-piperidyl)methyl}amino-6-oxohexyl)-3,3,3-triphenylpropanamide and ethyl iodide. The compound was obtained as a pale yellow solid.

Workup

customThe compound was obtained as a pale yellow solid

Sources & evidence

ORD record: ord-f97e6306233f4e1880832bff9b94b251
Source dataset: uspto-grants-2004_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06809108B1

Reaction notes

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