Dimethylformamide → HCID 74372495, compound

HRID 2138740Notes

Reaction equation

HRID 2138740 reaction equation
[Br:25][c:26]1[cH:27][n:28][c:29]([NH:31][C:32]([O:33][C:34]([CH3:35])([CH3:36])[CH3:37])=[O:38])[s:30]1.[CH3:1][S:2](=[N:3][C:4]([c:5]1[cH:6][n:7][cH:8][c:9]([C:11]#[C:12][Si:13]([CH3:14])([CH3:15])[CH3:16])[cH:10]1)=[O:17])([c:18]1[cH:19][cH:20][cH:21][cH:22][cH:23]1)=[O:24].[CH3:58][CH2:59][N:60]([CH2:61][CH3:62])[CH2:63][CH3:64].[CH3:66][CH2:67][CH2:68][CH2:69][N+:70]([CH2:71][CH2:72][CH2:73][CH3:74])([CH2:75][CH2:76][CH2:77][CH3:78])[CH2:79][CH2:80][CH2:81][CH3:82].[Cu:129][I:130].[F-:65].[O:83]=[CH:84][N:85]([CH3:86])[CH3:87].[Pd:88]([Cl:89])[Cl:90].[c:110]1([P:111]([c:112]2[cH:113][cH:114][cH:115][cH:116][cH:117]2)[c:118]2[cH:119][cH:120][cH:121][cH:122][cH:123]2)[cH:124][cH:125][cH:126][cH:127][cH:128]1.[c:39]1([P:40]([c:41]2[cH:42][cH:43][cH:44][cH:45][cH:46]2)[c:47]2[cH:48][cH:49][cH:50][cH:51][cH:52]2)[cH:53][cH:54][cH:55][cH:56][cH:57]1.[c:91]1([P:92]([c:93]2[cH:94][cH:95][cH:96][cH:97][cH:98]2)[c:99]2[cH:100][cH:101][cH:102][cH:103][cH:104]2)[cH:105][cH:106][cH:107][cH:108][cH:109]1>>[CH3:1][S:2](=[N:3][C:4]([c:5]1[cH:6][n:7][cH:8][c:9]([C:11]#[C:12][c:26]2[cH:27][n:28][c:29]([NH:31][C:32]([O:33][C:34]([CH3:35])([CH3:36])[CH3:37])=[O:38])[s:30]2)[cH:10]1)=[O:17])([c:18]1[cH:19][cH:20][cH:21][cH:22][cH:23]1)=[O:24]

Participants

10

Reactant 9

HCID 6228DimethylformamideHCID 8471TriethylamineHCID 11776Triphenylphosphine3×HCID 16028TetrabutylammoniumHCID 24290Palladium ChlorideHCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 28179Fluoride IonHCID 21300388tert-butyl N-(5-bromo-1,3-thiazol-2-yl)carbamateHCID 57657915N-[methyl(oxo)phenyl-lambda6-sulfanylidene]-5-[(trimethylsilyl)ethynyl]nicotinamide

Product 1

HCID 74372495HCID 74372495, compound

Sources & evidence

ORD record
ord-30ee24000d0647a3949d2f8170aab084
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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