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Chloride → N-(3-((5-(4-cyanophenyl)thiazol-2-yl)amino)phenyl)methanesulfonamide

HRID 118048
Notes
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Reaction equation

HRID 118048 reaction equation
[Br:1][c:2]1[cH:3][n:4][c:5]([NH:7][c:8]2[cH:9][c:10]([NH:14][S:15](=[O:16])(=[O:17])[CH3:18])[cH:11][cH:12][cH:13]2)[s:6]1.[C:38](=[O:39])([O-:40])[O-:41].[CH3:19][C:20]1([CH3:21])[C:22]([CH3:23])([CH3:24])[O:25][B:26]([c:27]2[cH:28][cH:29][c:30]([C:31]#[N:32])[cH:33][cH:34]2)[O:35]1.[CH3:44][CH2:45][CH2:46][CH2:47][CH2:48][CH3:49].[Cl-:37].[Li+:36].[Na+:42].[Na+:43].[cH:50]1[cH:51][cH:52][c:53]([P:54]([Pd:55]([P:56]([c:57]2[cH:58][cH:59][cH:60][cH:61][cH:62]2)([c:63]2[cH:64][cH:65][cH:66][cH:67][cH:68]2)[c:69]2[cH:70][cH:71][cH:72][cH:73][cH:74]2)([P:75]([c:76]2[cH:77][cH:78][cH:79][cH:80][cH:81]2)([c:82]2[cH:83][cH:84][cH:85][cH:86][cH:87]2)[c:88]2[cH:89][cH:90][cH:91][cH:92][cH:93]2)[P:94]([c:95]2[cH:96][cH:97][cH:98][cH:99][cH:100]2)([c:101]2[cH:102][cH:103][cH:104][cH:105][cH:106]2)[c:107]2[cH:108][cH:109][cH:110][cH:111][cH:112]2)([c:113]2[cH:114][cH:115][cH:116][cH:117][cH:118]2)[c:119]2[cH:120][cH:121][cH:122][cH:123][cH:124]2)[cH:125][cH:126]1>>[c:2]1(-[c:27]2[cH:28][cH:29][c:30]([C:31]#[N:32])[cH:33][cH:34]2)[cH:3][n:4][c:5]([NH:7][c:8]2[cH:9][c:10]([NH:14][S:15](=[O:16])(=[O:17])[CH3:18])[cH:11][cH:12][cH:13]2)[s:6]1
ParticipantsSources & evidenceReaction notes

Participants

9

Reactant 8

HCID 312ChlorideHCID 923Sodium Ion2×HCID 8058HexaneHCID 19660Carbonate IonHCID 28486Lithium ionHCID 27346254-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 86674186
N-(3-((5-bromothiazol-2-yl)amino)phenyl)methanesulfonamide
HCID 178420554HCID 178420554, compound

Product 1

HCID 71471997N-(3-((5-(4-cyanophenyl)thiazol-2-yl)amino)phenyl)methanesulfonamide

Sources & evidence

ORD record
ord-584b1427ce0448a4a8a65bb9a2d6e784
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes