Lithium Hydroxide → 2-(3-(2-((2-Chlorophenyl)(methyl)carbamoyl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-8-yl)phenyl)acetic acid

HRID 2078868Notes

Reaction equation

HRID 2078868 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]([CH3:36])[C:9]([C:11]1[S:35][C:14]2[C:15]3[CH:23]=[CH:22][C:21]([C:24]4[CH:25]=[C:26]([CH2:30][C:31]([O:33]C)=[O:32])[CH:27]=[CH:28][CH:29]=4)=[CH:20][C:16]=3[O:17][CH2:18][CH2:19][C:13]=2[CH:12]=1)=[O:10].[OH-].[Li+]>C1COCC1.O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]([CH3:36])[C:9]([C:11]1[S:35][C:14]2[C:15]3[CH:23]=[CH:22][C:21]([C:24]4[CH:25]=[C:26]([CH2:30][C:31]([OH:33])=[O:32])[CH:27]=[CH:28][CH:29]=4)=[CH:20][C:16]=3[O:17][CH2:18][CH2:19][C:13]=2[CH:12]=1)=[O:10]

Participants

5

Procedure

Methyl 2-(3-(2-((2-chlorophenyl)(methyl)carbamoyl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-8-yl)phenyl)acetate 200 was treated with lithium hydroxide in THF and water to give 198. MS: (ESI+) 503.7

Sources & evidence

ORD record
ord-0ea18693a4f3437793f1c132d79d26fa
Source dataset
uspto-grants-2011_04
Patent number
US07928248B2

Reaction notes

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