2-Bromo-4-(bromomethyl)-1-(trifluoromethyl)benzene → HCID 86685279, compound

HRID 402834Notes

Reaction equation

HRID 402834 reaction equation
Cl.[O:2]=[C:3]1[N:7]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=2)[CH2:6][C:5]2([CH2:22][CH2:21][NH:20][CH2:19][CH2:18]2)[O:4]1.[Br:23][C:24]1[CH:29]=[C:28]([CH2:30]Br)[CH:27]=[CH:26][C:25]=1[C:32]([F:35])([F:34])[F:33]>>[Br:23][C:24]1[CH:29]=[C:28]([CH:27]=[CH:26][C:25]=1[C:32]([F:33])([F:34])[F:35])[CH2:30][N:20]1[CH2:21][CH2:22][C:5]2([O:4][C:3](=[O:2])[N:7]([C:8]3[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=3)[CH2:6]2)[CH2:18][CH2:19]1

Participants

3

Reactant 2

HCID 180009852-Bromo-4-(bromomethyl)-1-(trifluoromethyl)benzeneHCID 66764605Methyl 4-(2-oxo-1-oxa-3,8-diazaspiro[4.5]dec-3-yl)benzoate hydrochloride salt

Product 1

HCID 86685279HCID 86685279, compound

Procedure

The title compound was prepared from methyl 4-(2-oxo-1-oxa-3,8-diazaspiro[4.5]dec-3-yl)benzoate hydrochloride salt (50 mg, 0.153 mmol; Example 1, Step 2) and 2-bromo-4-(bromomethyl)-1-(trifluoromethyl)benzene (53.5 mg, 0.168 mmol) following essentially the same procedure described in Step 1 of Example 7-9. The title compound was obtained as a yellow oil (91 mg) that was used without any further purification.

Sources & evidence

ORD record
ord-efa7320416e640fea1c8283aa576ba42
Source dataset
uspto-grants-2014_06
Patent number
US08742110B2

Reaction notes

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