2-Bromo-4-methylanisole → HCID 56655614, compound

HRID 1039003Notes

Reaction equation

HRID 1039003 reaction equation
[F:1][C:2]([F:22])([F:21])[O:3][C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:14][CH2:13][C:12]3([CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)[C:11]2=[O:20])=[CH:6][CH:5]=1.Br[C:24]1[CH:29]=[C:28]([CH3:30])[CH:27]=[CH:26][C:25]=1[O:31][CH3:32]>>[CH3:32][O:31][C:25]1[CH:26]=[CH:27][C:28]([CH3:30])=[CH:29][C:24]=1[N:17]1[CH2:16][CH2:15][C:12]2([C:11](=[O:20])[N:10]([C:7]3[CH:8]=[CH:9][C:4]([O:3][C:2]([F:1])([F:21])[F:22])=[CH:5][CH:6]=3)[CH2:14][CH2:13]2)[CH2:19][CH2:18]1

Participants

3

Reactant 2

HCID 891432-Bromo-4-methylanisoleHCID 667427592-(4-(Trifluoromethoxy)phenyl)-2,8-diazaspiro[4.5]decan-1-one

Product 1

HCID 56655614HCID 56655614, compound

Procedure

The title compound was prepared in analogy to example 1 step D from a mixture of 2-(4-trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decan-1-one (described in example 1 step C) and 2-bromo-4-methylanisole. Light yellow solid. MS (ESI): 435.3 (MH+)

Sources & evidence

ORD record
ord-302d6401b356458c84017657b4fc7904
Source dataset
uspto-grants-2013_10
Patent number
US08552024B2

Reaction notes

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