Tetrahydrofuran → 5-Chloro-1H-pyrrolo[2,3-b]pyridine

HRID 676679Notes

Reaction equation

[Br:18][c:19]1[c:20]2[c:21]([n:22][cH:23][cH:24][cH:25]2)[n:26]([S:27]([c:28]2[cH:29][cH:30][c:31]([CH3:32])[cH:33][cH:34]2)(=[O:35])=[O:36])[cH:37]1.[CH2:39]([N+:40]([CH2:41][CH2:42][CH2:43][CH3:44])([CH2:45][CH2:46][CH2:47][CH3:48])[CH2:49][CH2:50][CH2:51][CH3:52])[CH2:53][CH2:54][CH3:55].[CH2:56]1[O:57][CH2:58][CH2:59][CH2:60]1.[CH3:61][CH2:62][O:63][C:64](=[O:65])[CH3:66].[Cl:1][c:2]1[cH:3][c:4]2[c:5]([n:6][cH:7]1)[nH:8][c:9]([Si:11]([CH2:12][CH3:13])([CH2:14][CH3:15])[CH2:16][CH3:17])[cH:10]2.[F-:38]>>[Cl:1][c:2]1[cH:3][c:4]2[c:5]([n:6][cH:7]1)[nH:8][cH:9][cH:10]2

Participants

Reactant 6

HCID 8028Tetrahydrofuran

HCID 8857Ethyl Acetate

HCID 16028Tetrabutylammonium

HCID 28179Fluoride Ion

HCID 216691553-Bromo-1-(4-methylbenzene-1-sulfonyl)-1H-pyrrolo[2,3-b]pyridine

HCID 57774343HCID 57774343, compound

Product 1

HCID 242292135-Chloro-1H-pyrrolo[2,3-b]pyridine

Sources & evidence

ORD record: ord-77c08c4dbc034ab5953611e52055acb1
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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