4-Bromo-2-chlorophenol → HCID 59243622, compound

HRID 425023Notes

Reaction equation

HRID 425023 reaction equation
[C:1]([O:5][C:6]([NH:8][C@H:9]([C:28]([O:30][CH:31]1[CH2:35][CH2:34][CH2:33][CH2:32]1)=[O:29])[CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([B:19]2[O:23][C:22]([CH3:25])([CH3:24])[C:21]([CH3:27])([CH3:26])[O:20]2)=[CH:15][CH:14]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].BrC1C=CC(O)=C([Cl:44])C=1>>[C:1]([O:5][C:6]([NH:8][C@H:9]([C:28]([O:30][CH:31]1[CH2:32][CH2:33][CH2:34][CH2:35]1)=[O:29])[CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([B:19]2[O:20][C:21]([CH3:26])([CH3:27])[C:22]([CH3:25])([CH3:24])[O:23]2)=[CH:15][C:14]=1[Cl:44])=[O:7])([CH3:2])([CH3:3])[CH3:4]

Participants

3

Reactant 2

HCID 198594-Bromo-2-chlorophenolHCID 59243600HCID 59243600, compound

Product 1

HCID 59243622HCID 59243622, compound

Procedure

Synthesised by analogous methods to Intermediate 2b, using 4-bromo-2-chloro-phenol at Stage 6 of Scheme 2. m/z 524 [M+H]+.

Sources & evidence

ORD record
ord-8a121a3b53c54e3a9e84c2070bde6a7d
Source dataset
uspto-grants-2012_01
Patent number
US08106091B2

Reaction notes

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