HCID 57443758, compound → HCID 57589078, compound

HRID 1782788Notes

Reaction equation

HRID 1782788 reaction equation
[CH2:1]([O:3][C:4](=[O:23])[CH2:5][CH:6]1[CH2:9][N:8]([C:10]([C:12]2[CH:13]=[C:14]([CH:19]=[CH:20][C:21]=2[OH:22])[C:15]([O:17][CH3:18])=[O:16])=[O:11])[CH2:7]1)[CH3:2].Br[CH2:25][CH2:26][CH2:27][C:28]1[CH:33]=[CH:32][C:31]([O:34][CH2:35][CH2:36][CH2:37][CH:38]2[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]2)=[CH:30][CH:29]=1>>[CH:38]1([CH2:37][CH2:36][CH2:35][O:34][C:31]2[CH:32]=[CH:33][C:28]([CH2:27][CH2:26][CH2:25][O:22][C:21]3[CH:20]=[CH:19][C:14]([C:15]([O:17][CH3:18])=[O:16])=[CH:13][C:12]=3[C:10]([N:8]3[CH2:7][CH:6]([CH2:5][C:4]([O:3][CH2:1][CH3:2])=[O:23])[CH2:9]3)=[O:11])=[CH:29][CH:30]=2)[CH2:39][CH2:40][CH2:41][CH2:42][CH2:43]1

Participants

3

Reactant 2

HCID 57443758HCID 57443758, compoundHCID 69077746HCID 69077746, compound

Product 1

HCID 57589078HCID 57589078, compound

Procedure

Preparation takes place in analogy to the process described in Example 22 from methyl 3-{[3-(2-ethoxy-2-oxoethyl)azetidin-1-yl]carbonyl}-4-hydroxybenzoate and 1-(3-bromopropyl)-4-(3-cyclohexylpropoxy)benzene.

Workup

  1. customPreparation

Sources & evidence

ORD record
ord-ba946eb641c849c2b4a88f9bf35c44f4
Source dataset
uspto-grants-2009_03
Patent number
US07498460B2

Reaction notes

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