Phenethyl bromide → HCID 11627082, compound

HRID 1453729Notes

Reaction equation

HRID 1453729 reaction equation
C([O:5][C:6](=[O:30])[CH2:7][N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]([CH:17]2[C:21]3[CH:22]=[CH:23][C:24]([F:26])=[CH:25][C:20]=3[S:19](=[O:28])(=[O:27])[NH:18]2)=[C:9]1[CH3:29])(C)(C)C.[CH:31]1[CH:36]=[CH:35][C:34]([CH2:37][CH2:38]Br)=[CH:33][CH:32]=1>>[F:26][C:24]1[CH:23]=[CH:22][C:21]2[CH:17]([C:10]3[C:11]4[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=4)[N:8]([CH2:7][C:6]([OH:5])=[O:30])[C:9]=3[CH3:29])[N:18]([CH2:38][CH2:37][C:34]3[CH:35]=[CH:36][CH:31]=[CH:32][CH:33]=3)[S:19](=[O:28])(=[O:27])[C:20]=2[CH:25]=1

Participants

3

Procedure

The title compound was prepared by the method described for example 14 using the product from example 13, step e) and 2-phenethyl bromide. MS: ESI (negative): 477 (M−H).

Sources & evidence

ORD record
ord-ecafc41f000f4a0aaac6f207b001f66c
Source dataset
uspto-grants-2009_01
Patent number
US07476667B2

Reaction notes

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