2-(Azetidin-1-ylcarbonyl)-5-bromopyridine → HCID 59127161, compound

HRID 1011810Notes

Reaction equation

HRID 1011810 reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([O:12][C@@H:13]([CH3:16])[CH2:14][OH:15])[CH:11]=1)[C:5]([O:7]C)=[O:6].[N:17]1([C:21]([C:23]2[CH:28]=[CH:27][C:26](Br)=[CH:25][N:24]=2)=[O:22])[CH2:20][CH2:19][CH2:18]1>>[N:17]1([C:21]([C:23]2[N:24]=[CH:25][C:26]([O:1][C:2]3[CH:3]=[C:4]([CH:9]=[C:10]([O:12][C@@H:13]([CH3:16])[CH2:14][OH:15])[CH:11]=3)[C:5]([OH:7])=[O:6])=[CH:27][CH:28]=2)=[O:22])[CH2:20][CH2:19][CH2:18]1

Participants

3

Reactant 2

HCID 536296172-(Azetidin-1-ylcarbonyl)-5-bromopyridineHCID 59127187methyl 3-hydroxy-5-[(1S)-2-hydroxy-1-methylethoxy]benzoate

Product 1

HCID 59127161HCID 59127161, compound

Procedure

The preparations of methyl 3-hydroxy-5-[(1S)-2-hydroxy-1-methylethoxy]benzoate and 2-(azetidin-1-ylcarbonyl)-5-bromopyridine were described earlier.

Sources & evidence

ORD record
ord-0bf67c260afa425a842c22726a187140
Source dataset
uspto-grants-2011_07
Patent number
US07977328B2

Reaction notes

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