Hydrochloric Acid → HCID 11610950, compound

HRID 1445789Notes

Reaction equation

HRID 1445789 reaction equation
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8](B(O)O)=[CH:7][CH:6]=1)(=[O:4])=[O:3].Br[C:15]1[CH:20]=[CH:19][C:18]([C:21]2[O:22][CH:23]=[C:24]([CH2:26][N:27]3[CH2:31][CH2:30][CH2:29][CH:28]3[CH3:32])[N:25]=2)=[CH:17][CH:16]=1.Cl>>[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([C:15]2[CH:20]=[CH:19][C:18]([C:21]3[O:22][CH:23]=[C:24]([CH2:26][N:27]4[CH2:31][CH2:30][CH2:29][CH:28]4[CH3:32])[N:25]=3)=[CH:17][CH:16]=2)=[CH:7][CH:6]=1)(=[O:4])=[O:3]

Participants

4

Procedure

The titled compound is prepared substantially in accordance with the procedure of Example 4 using 4-methylsulfonylphenylboronic acid and (+/−)-2-(4-Bromo-phenyl)-4-(2-methyl-pyrrolidin-1-ylmethyl)-oxazole; hydrochloride (See Example 5). MS (m/e) 397.1 (M+1)

Sources & evidence

ORD record
ord-871d3a5ff7984bc98290eb77e72e43ec
Source dataset
uspto-grants-2010_02
Patent number
US07666871B2

Reaction notes

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