Methyl iodide → HCID 58651297, compound

HRID 1832553Notes

Reaction equation

[C:1]([C:4]1[CH:5]=[C:6]([CH:35]=[CH:36][CH:37]=1)[O:7][C@@H:8]([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[CH2:9][CH2:10][N:11]1[CH2:16][CH2:15][CH:14]([C:17]2[CH:18]=[C:19]([NH:23][C:24](=[O:28])[CH:25]([CH3:27])[CH3:26])[CH:20]=[CH:21][CH:22]=2)[CH2:13][CH2:12]1)(=[O:3])[CH3:2].[CH3:38]I>>[C:1]([C:4]1[CH:5]=[C:6]([CH:35]=[CH:36][CH:37]=1)[O:7][C@@H:8]([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[CH2:9][CH2:10][N:11]1[CH2:16][CH2:15][CH:14]([C:17]2[CH:18]=[C:19]([N:23]([CH3:38])[C:24](=[O:28])[CH:25]([CH3:27])[CH3:26])[CH:20]=[CH:21][CH:22]=2)[CH2:13][CH2:12]1)(=[O:3])[CH3:2]

Participants

Reactant 2

HCID 6328Methyl iodide

HCID 10074641HCID 10074641, compound

Product 1

HCID 58651297HCID 58651297, compound

Procedure

Prepared by Procedure T and Scheme AD using N-(3-{1-[(3R)-3-(3-acetylphenoxy)-3-phenylpropyl]-4-piperidinyl}phenyl)-2-methylpropanamide and methyl iodide: ESMS m/e: 513.2 (M+H)+.

Workup

customPrepared by Procedure T and Scheme AD

Sources & evidence

ORD record: ord-ee41be0b2ae34ede8d1d78d5cf05b6c8
Source dataset: uspto-grants-2006_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07067534B1

Reaction notes

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