tert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylate → HCID 71074835, compound

HRID 1851953Notes

Reaction equation

HRID 1851953 reaction equation
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]([O:13][CH3:14])=[O:12])[CH:9]=2)[NH:4][CH:3]=1.Br[CH2:16][C:17]1[CH:22]=[CH:21][C:20]([C:23]2[C:24]([C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])=[CH:25][CH:26]=[CH:27][CH:28]=2)=[CH:19][CH:18]=1>>[C:32]([O:31][C:29]([C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=1[C:20]1[CH:21]=[CH:22][C:17]([CH2:16][N:4]2[C:5]3[C:10](=[CH:9][C:8]([C:11]([O:13][CH3:14])=[O:12])=[CH:7][CH:6]=3)[C:2]([CH3:1])=[CH:3]2)=[CH:18][CH:19]=1)=[O:30])([CH3:35])([CH3:34])[CH3:33]

Participants

3

Reactant 2

HCID 9906257tert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylateHCID 23383527Methyl 3-methyl-1H-indole-5-carboxylate

Product 1

HCID 71074835HCID 71074835, compound

Procedure

The title compound was prepared following the same protocol as described in Step 2, Example 38, using the methyl 3-methyl-1H-indole-5-carboxylate instead of the methyl 1H-indole-5-carboxylate, and the tert-butyl 4′-(bromomethyl)biphenyl-2-carboxylate instead of the 1-bromo-4-(bromomethyl)benzene. ESI-MS (m/z): 456 [M+H]+.

Sources & evidence

ORD record
ord-30cc932c87a04e24a81ec4cca703a70e
Source dataset
uspto-grants-2015_02
Patent number
US08957093B2

Reaction notes

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