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2-bromo-N-(pyrazin-2-yl)acetamide → Bromide ion

HRID 1203435
Notes
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Reaction equation

HRID 1203435 reaction equation
[Br:25][CH2:26][C:27](=[O:28])[NH:29][c:30]1[n:31][cH:32][cH:33][n:34][cH:35]1.[c:1]1([C:7]2([C:14](=[O:15])[O:16][CH:17]3[CH2:18][N:19]4[CH2:20][CH2:21][CH:22]3[CH2:23][CH2:24]4)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1>>[Br-:25].[c:1]1([C:7]2([C:14](=[O:15])[O:16][CH:17]3[CH2:18][N+:19]4([CH2:26][C:27](=[O:28])[NH:29][c:30]5[n:31][cH:32][cH:33][n:34][cH:35]5)[CH2:20][CH2:21][CH:22]3[CH2:23][CH2:24]4)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1
ParticipantsSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 445426692-bromo-N-(pyrazin-2-yl)acetamideHCID 668858941-Azabicyclo[2.2.2]octan-3-yl 1-phenylcycloheptane-1-carboxylate

Product 2

HCID 259Bromide ionHCID 74380986HCID 74380986, compound

Sources & evidence

ORD record
ord-7e6122bd52ab409f99deec22204a2e9a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes