Tetrahydrofuran → HCID 136337804, compound

HRID 172755Notes

Reaction equation

[CH2:46]1[O:47][CH2:48][CH2:49][CH2:50]1.[CH3:29][CH2:30][CH2:31][CH2:32][N+:33]([CH2:34][CH2:35][CH2:36][CH3:37])([CH2:38][CH2:39][CH2:40][CH3:41])[CH2:42][CH2:43][CH2:44][CH3:45].[F-:28].[n:1]1[n:2][c:3](-[c:10]2[n:11][c:12]3[c:13]([O:20][Si:21]([C:22]([CH3:23])([CH3:24])[CH3:25])([CH3:26])[CH3:27])[cH:14][cH:15][cH:16][c:17]3[cH:18][cH:19]2)[n:4]2[c:5]1[cH:6][cH:7][cH:8][cH:9]2>>[n:1]1[n:2][c:3](-[c:10]2[n:11][c:12]3[c:13]([OH:20])[cH:14][cH:15][cH:16][c:17]3[cH:18][cH:19]2)[n:4]2[c:5]1[cH:6][cH:7][cH:8][cH:9]2

Participants

Reactant 4

HCID 8028Tetrahydrofuran

HCID 16028Tetrabutylammonium

HCID 28179Fluoride Ion

HCID 672314422-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)-8-(tert-butyldimethylsilyloxy) quinoline

Product 1

HCID 136337804HCID 136337804, compound

Sources & evidence

ORD record: ord-df427df7fb904c84a03318ac91940712
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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