4-[(4-Bromobenzene)sulfonyl]morpholine → HCID 44608154, compound

HRID 1967162Notes

Reaction equation

HRID 1967162 reaction equation
[NH2:1][C:2]1[S:3][C:4]([C:10]2[C:15]([F:16])=[CH:14][C:13]([C:17]([OH:20])([CH3:19])[CH3:18])=[CH:12][C:11]=2[F:21])=[CH:5][C:6]=1[C:7]([NH2:9])=[O:8].Br[C:23]1[CH:28]=[CH:27][C:26]([S:29]([N:32]2[CH2:37][CH2:36][O:35][CH2:34][CH2:33]2)(=[O:31])=[O:30])=[CH:25][CH:24]=1>>[F:16][C:15]1[CH:14]=[C:13]([C:17]([OH:20])([CH3:18])[CH3:19])[CH:12]=[C:11]([F:21])[C:10]=1[C:4]1[S:3][C:2]([NH:1][C:23]2[CH:28]=[CH:27][C:26]([S:29]([N:32]3[CH2:33][CH2:34][O:35][CH2:36][CH2:37]3)(=[O:30])=[O:31])=[CH:25][CH:24]=2)=[C:6]([C:7]([NH2:9])=[O:8])[CH:5]=1

Participants

3

Procedure

5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-{[4-(morpholin-4-ylsulfonyl)phenyl]amino}thiophene-3-carboxamide was prepared according to the general procedure in Example 1 using 2-amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (150 mg, 0.480 mmol) and 4-[(4-bromophenyl)sulfonyl]morpholine (147 mg, 0.480 mmol) as the starting materials.

Sources & evidence

ORD record
ord-bfa45d07708840969d6ba41efa4d42e0
Source dataset
uspto-grants-2013_04
Patent number
US08420695B2

Reaction notes

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