Benzyl Bromide → HCID 25027936, compound

HRID 1864475Notes

Reaction equation

HRID 1864475 reaction equation
[CH:1]1([S:4]([N:7]2[CH2:11][C@@H:10]([C:12]([N:14]3[CH2:19][CH2:18][N:17]([C:20]4[CH:25]=[C:24]([CH3:26])[CH:23]=[CH:22][C:21]=4[CH3:27])[CH2:16][CH2:15]3)=[O:13])[NH:9][C:8]2=[O:28])(=[O:6])=[O:5])[CH2:3][CH2:2]1.[CH2:29](Br)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>>[CH2:29]([N:9]1[C@H:10]([C:12]([N:14]2[CH2:19][CH2:18][N:17]([C:20]3[CH:25]=[C:24]([CH3:26])[CH:23]=[CH:22][C:21]=3[CH3:27])[CH2:16][CH2:15]2)=[O:13])[CH2:11][N:7]([S:4]([CH:1]2[CH2:3][CH2:2]2)(=[O:5])=[O:6])[C:8]1=[O:28])[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1

Participants

3

Reactant 2

HCID 7498Benzyl BromideHCID 67140901HCID 67140901, compound

Product 1

HCID 25027936HCID 25027936, compound

Procedure

In analogy to example 66, step 4, from (S)-1-cyclopropanesulfonyl-4-[4-(2,5-dimethyl-phenyl)-piperazine-1-carbonyl]-imidazolidin-2-one and benzyl bromide was prepared

Sources & evidence

ORD record
ord-fb3d6bd0a50e4996b6da6a4bded798b3
Source dataset
uspto-grants-2009_12
Patent number
US07625902B2

Reaction notes

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