Methyl iodide → HCID 86662775, compound

HRID 1810581Notes

Reaction equation

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

Participants

Reactant 2

HCID 6328Methyl iodide

HCID 86662776HCID 86662776, compound

Product 1

HCID 86662775HCID 86662775, compound

Procedure

Prepared according to the procedure described in Example 213, Step 5, using the following starting materials: {2′-[(acetyl-ethyl-amino)-methyl]-5,4′-bis-trifluoromethyl-biphenyl-3-yl}-acetic acid ethyl ester and iodomethane.

Workup

customPrepared

Sources & evidence

ORD record: ord-33f33020b6f54aa284d9eb28e577a843
Source dataset: uspto-grants-2013_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08362044B2

Reaction notes

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