Carbonate Ion → HCID 67776770, compound

HRID 1550427Notes

Reaction equation

HRID 1550427 reaction equation
[Br:1][c:2]1[cH:3][c:4]2[n:5]([cH:6][cH:7]1)[n:8][c:9]([N:11]1[CH2:12][CH2:13][O:14][CH2:15][CH2:16]1)[n:10]2.[C:17]([NH2:18])([O:19][C:20]([CH3:21])([CH3:22])[CH3:23])=[O:24].[C:67](=[O:68])([O-:69])[O-:70].[Cs+:71].[Cs+:72].[O:117]=[C:118]([CH:119]=[CH:120][c:121]1[cH:122][cH:123][cH:124][cH:125][cH:126]1)[CH:127]=[CH:128][c:129]1[cH:130][cH:131][cH:132][cH:133][cH:134]1.[O:73]1[CH2:74][CH2:75][O:76][CH2:77][CH2:78]1.[O:81]=[C:82]([CH:83]=[CH:84][c:85]1[cH:86][cH:87][cH:88][cH:89][cH:90]1)[CH:91]=[CH:92][c:93]1[cH:94][cH:95][cH:96][cH:97][cH:98]1.[O:99]=[C:100]([CH:101]=[CH:102][c:103]1[cH:104][cH:105][cH:106][cH:107][cH:108]1)[CH:109]=[CH:110][c:111]1[cH:112][cH:113][cH:114][cH:115][cH:116]1.[Pd:79].[Pd:80].[c:25]1([P:26]([c:27]2[cH:28][cH:29][cH:30][cH:31][cH:32]2)[c:33]2[c:34]3[c:58]([cH:59][cH:60][cH:61]2)[C:55]([CH3:56])([CH3:57])[c:37]2[c:36]([c:41]([P:42]([c:43]4[cH:44][cH:45][cH:46][cH:47][cH:48]4)[c:49]4[cH:50][cH:51][cH:52][cH:53][cH:54]4)[cH:40][cH:39][cH:38]2)[O:35]3)[cH:62][cH:63][cH:64][cH:65][cH:66]1>>[c:2]1([NH:18][C:17]([O:19][C:20]([CH3:21])([CH3:22])[CH3:23])=[O:24])[cH:3][c:4]2[n:5]([cH:6][cH:7]1)[n:8][c:9]([N:11]1[CH2:12][CH2:13][O:14][CH2:15][CH2:16]1)[n:10]2

Participants

9

Reactant 8

HCID 19660Carbonate IonHCID 23938Palladium2×HCID 312751,4-DioxaneHCID 77922tert-Butyl carbamateHCID 95417Dibenzylidene acetone3×HCID 104967Cesium cation2×HCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 677768607-Bromo-2-(4-morpholinyl)[1,2,4]triazolo[1,5-a]pyridine

Product 1

HCID 67776770HCID 67776770, compound

Sources & evidence

ORD record
ord-16540cb44d0e4b48831c142e0984c24e
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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