Ethanol → HCID 17962900, compound

HRID 665646Notes

Reaction equation

HRID 665646 reaction equation
[C:1]([CH3:2])(=[O:3])[N:4]1[C:5]([CH3:32])([CH3:33])[CH2:6][C:7]([CH3:25])([c:26]2[cH:27][cH:28][cH:29][cH:30][cH:31]2)[c:8]2[cH:9][c:10]([NH:14][C:15]([c:16]3[c:17]([Br:23])[c:18]([CH3:22])[cH:19][cH:20][cH:21]3)=[O:24])[cH:11][cH:12][c:13]21.[CH2:64]([OH:65])[CH3:66].[CH2:67]([CH2:68][O:69][CH3:70])[O:71][CH3:72].[Cs+:44].[F-:43].[O:111]=[C:112]([CH:113]=[CH:114][c:115]1[cH:116][cH:117][cH:118][cH:119][cH:120]1)[CH:121]=[CH:122][c:123]1[cH:124][cH:125][cH:126][cH:127][cH:128]1.[O:75]=[C:76]([CH:77]=[CH:78][c:79]1[cH:80][cH:81][cH:82][cH:83][cH:84]1)[CH:85]=[CH:86][c:87]1[cH:88][cH:89][cH:90][cH:91][cH:92]1.[O:93]=[C:94]([CH:95]=[CH:96][c:97]1[cH:98][cH:99][cH:100][cH:101][cH:102]1)[CH:103]=[CH:104][c:105]1[cH:106][cH:107][cH:108][cH:109][cH:110]1.[Pd:73].[Pd:74].[c:34]1([B:40]([OH:41])[OH:42])[cH:35][cH:36][cH:37][cH:38][cH:39]1.[c:45]1([P:46]([c:47]2[cH:48][cH:49][cH:50][cH:51][cH:52]2)[c:53]2[cH:54][cH:55][cH:56][cH:57][cH:58]2)[cH:59][cH:60][cH:61][cH:62][cH:63]1>>[C:1]([CH3:2])(=[O:3])[N:4]1[C:5]([CH3:32])([CH3:33])[CH2:6][C:7]([CH3:25])([c:26]2[cH:27][cH:28][cH:29][cH:30][cH:31]2)[c:8]2[cH:9][c:10]([NH:14][C:15]([c:16]3[c:17](-[c:34]4[cH:35][cH:36][cH:37][cH:38][cH:39]4)[c:18]([CH3:22])[cH:19][cH:20][cH:21]3)=[O:24])[cH:11][cH:12][c:13]21

Participants

10

Reactant 9

HCID 702EthanolHCID 80711,2-DimethoxyethaneHCID 11776TriphenylphosphineHCID 23938Palladium2×HCID 28179Fluoride IonHCID 66827Phenylboronic AcidHCID 95417Dibenzylidene acetone3×HCID 104967Cesium cationHCID 179629031-Acetyl-4-phenyl-6-(2-bromo-3-methylbenzoyl)amino-1,2,3,4-tetrahydro-2,2,4-trimethylquinoline

Product 1

HCID 17962900HCID 17962900, compound

Sources & evidence

ORD record
ord-0c5c84111689437587c926414d7f1314
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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