4-Fluorobenzyl bromide → HCID 59263352, compound

HRID 2323212Notes

Reaction equation

HRID 2323212 reaction equation
[CH3:1][C:2]1([CH3:23])[c:3]2[c:4]([cH:7][c:8]3[c:12]([cH:13]2)[C:11]2([CH2:10][O:9]3)[C:14](=[O:22])[NH:15][c:16]3[cH:17][cH:18][cH:19][cH:20][c:21]32)[O:5][CH2:6]1.[F:70][c:71]1[cH:72][cH:73][c:74]([CH2:75][Br:76])[cH:77][cH:78]1.[NH:24]1[c:25]2[c:26]([cH:27][cH:28][cH:29][cH:30]2)[C:31]2([c:32]3[cH:33][c:34]4[c:38]([cH:39][c:40]3[O:41][CH2:42]2)[O:37][CH2:36][O:35]4)[C:43]1=[O:44].[S:45]([O:46][CH2:56][CH:57]1[CH2:58][CH2:59][N:60]([C:63](=[O:64])[O:65][C:66]([CH3:67])([CH3:68])[CH3:69])[CH2:61][CH2:62]1)([c:47]1[cH:48][cH:49][c:50]([CH3:51])[cH:52][cH:53]1)(=[O:54])=[O:55]>>[CH3:1][C:2]1([CH3:23])[c:3]2[c:4]([cH:7][c:8]3[c:12]([cH:13]2)[C:11]2([CH2:10][O:9]3)[C:14](=[O:22])[N:15]([CH2:56][CH:57]3[CH2:58][CH2:59][N:60]([C:63](=[O:64])[O:65][C:66]([CH3:67])([CH3:68])[CH3:69])[CH2:61][CH2:62]3)[c:16]3[cH:17][cH:18][cH:19][cH:20][c:21]32)[O:5][CH2:6]1

Participants

5

Reactant 4

HCID 680214-Fluorobenzyl bromideHCID 106428511-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidineHCID 53375495spiro[furo[2,3-f][1,3]benzodioxole-7,3'-indol]-2'(1'H)-oneHCID 592634705,5-dimethyl-5,6-dihydrospiro[benzo[1,2-b:5,4-b']difuran-3,3'-indol]-2'(1H)-one

Product 1

HCID 59263352HCID 59263352, compound

Sources & evidence

ORD record
ord-ae0dc7b1ec774271976083abbf6c515c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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