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Potassium Cation → N,N-diethyl-5-(1-methyl-1H-indol-2-yl)pyridine-3-sulfonamide

HRID 118044
Notes
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Reaction equation

HRID 118044 reaction equation
[Br:14][c:15]1[cH:16][c:17]([S:21](=[O:22])(=[O:23])[N:24]([CH2:25][CH3:26])[CH2:27][CH3:28])[cH:18][n:19][cH:20]1.[CH2:120]1[O:121][CH2:122][CH2:123][O:124][CH2:125]1.[CH3:1][n:2]1[c:3]([B:11]([OH:12])[OH:13])[cH:4][c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]12.[K+:31].[K+:32].[N:29]#[N:30].[O-:33][C:34]([O-:35])=[O:36].[O:115]=[CH:116][N:117]([CH3:118])[CH3:119].[OH2:37].[cH:38]1[cH:39][cH:40][c:41]([P:42]([Pd:43]([P:44]([c:45]2[cH:46][cH:47][cH:48][cH:49][cH:50]2)([c:51]2[cH:52][cH:53][cH:54][cH:55][cH:56]2)[c:57]2[cH:58][cH:59][cH:60][cH:61][cH:62]2)([P:63]([c:64]2[cH:65][cH:66][cH:67][cH:68][cH:69]2)([c:70]2[cH:71][cH:72][cH:73][cH:74][cH:75]2)[c:76]2[cH:77][cH:78][cH:79][cH:80][cH:81]2)[P:82]([c:83]2[cH:84][cH:85][cH:86][cH:87][cH:88]2)([c:89]2[cH:90][cH:91][cH:92][cH:93][cH:94]2)[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)[cH:113][cH:114]1>>[CH3:1][n:2]1[c:3](-[c:15]2[cH:16][c:17]([S:21](=[O:22])(=[O:23])[N:24]([CH2:25][CH3:26])[CH2:27][CH3:28])[cH:18][n:19][cH:20]2)[cH:4][c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]12
ParticipantsSources & evidenceReaction notes

Participants

10

Reactant 9

HCID 813Potassium Cation2×HCID 947NitrogenHCID 962WaterHCID 6228DimethylformamideHCID 19660Carbonate IonHCID 312751,4-DioxaneHCID 198548155-Bromo-N,N-diethylpyridine-3-sulfonamide
HCID 22733820
(1-Methyl-1H-indol-2-yl)boronic acid
HCID 178420554HCID 178420554, compound

Product 1

HCID 58215618N,N-diethyl-5-(1-methyl-1H-indol-2-yl)pyridine-3-sulfonamide

Sources & evidence

ORD record
ord-c0eb6858df634632a307b0e0271840ef
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