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HCID 21099424, compound → HCID 21099431, compound

HRID 2376987
Notes
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Reaction equation

HRID 2376987 reaction equation
Br[C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5].[F:12][C:13]1[CH:18]=[C:17]([F:19])[CH:16]=[CH:15][C:14]=1[CH2:20][CH2:21][C:22]1[CH:27]=[CH:26][C:25]([S:28](C2C=CC=CC=2)(=[O:30])=[O:29])=[CH:24][CH:23]=1>>[F:12][C:13]1[CH:18]=[C:17]([F:19])[CH:16]=[CH:15][C:14]=1/[CH:20]=[CH:21]/[C:22]1[CH:27]=[CH:26][C:25]([S:28]([C:2]2[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=2[C:4]([NH2:6])=[O:5])(=[O:30])=[O:29])=[CH:24][CH:23]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 21099424HCID 21099424, compoundHCID 21779708HCID 21779708, compound

Product 1

HCID 21099431HCID 21099431, compound

Procedure

Prepared from 2-bromo-3-methylbenzamide by the procedure of Example 135 using Intermediate 2 in Step 2. m/z (ES+) 397 [(M-NH2)+].

Sources & evidence

ORD record
ord-9e06ed2adb9543bbb1636a06fc51b54a
Source dataset
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07468393B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes