Tetrahydrofuran → HCID 67165150, compound

HRID 1548649Notes

Reaction equation

HRID 1548649 reaction equation
[C:49](=[O:50])([O-:51])[O-:52].[CH2:1]([c:2]1[c:3]([NH:8][C:9]([CH2:10][O:11][CH2:12][C:13](=[O:14])[NH:15][c:16]2[c:17]([C:18](=[O:19])[O:20][CH3:21])[cH:22][c:23]([Br:26])[cH:24][cH:25]2)=[O:27])[cH:4][cH:5][cH:6][cH:7]1)[c:28]1[cH:29][cH:30][cH:31][cH:32][cH:33]1.[CH2:55]1[O:56][CH2:57][CH2:58][CH2:59]1.[CH3:34][C:35]1([CH3:36])[C:37]([CH3:38])([CH3:39])[O:40][B:41]([c:42]2[cH:43][cH:44][n:45][cH:46][cH:47]2)[O:48]1.[Cs+:53].[Cs+:54].[cH:60]1[cH:61][cH:62][c:63]([P:64]([Pd:65]([P:66]([c:67]2[cH:68][cH:69][cH:70][cH:71][cH:72]2)([c:73]2[cH:74][cH:75][cH:76][cH:77][cH:78]2)[c:79]2[cH:80][cH:81][cH:82][cH:83][cH:84]2)([P:85]([c:86]2[cH:87][cH:88][cH:89][cH:90][cH:91]2)([c:92]2[cH:93][cH:94][cH:95][cH:96][cH:97]2)[c:98]2[cH:99][cH:100][cH:101][cH:102][cH:103]2)[P:104]([c:105]2[cH:106][cH:107][cH:108][cH:109][cH:110]2)([c:111]2[cH:112][cH:113][cH:114][cH:115][cH:116]2)[c:117]2[cH:118][cH:119][cH:120][cH:121][cH:122]2)([c:123]2[cH:124][cH:125][cH:126][cH:127][cH:128]2)[c:129]2[cH:130][cH:131][cH:132][cH:133][cH:134]2)[cH:135][cH:136]1>>[CH2:1]([c:2]1[c:3]([NH:8][C:9]([CH2:10][O:11][CH2:12][C:13](=[O:14])[NH:15][c:16]2[c:17]([C:18](=[O:19])[O:20][CH3:21])[cH:22][c:23](-[c:42]3[cH:43][cH:44][n:45][cH:46][cH:47]3)[cH:24][cH:25]2)=[O:27])[cH:4][cH:5][cH:6][cH:7]1)[c:28]1[cH:29][cH:30][cH:31][cH:32][cH:33]1

Participants

7

Reactant 6

HCID 8028TetrahydrofuranHCID 19660Carbonate IonHCID 104967Cesium cation2×HCID 27346484-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 67163873HCID 67163873, compoundHCID 178420554HCID 178420554, compound

Product 1

HCID 67165150HCID 67165150, compound

Sources & evidence

ORD record
ord-40e626e6c9cb4229a158f0f71734617a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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