Tetrahydrofuran → HCID 49758988, compound

HRID 1551424Notes

Reaction equation

HRID 1551424 reaction equation
[CH3:26][c:27]1[cH:28][cH:29][c:30]([S:31](=[O:32])(=[O:33])[C:36]#[N:37])[cH:34][cH:35]1.[CH3:43][CH2:44][CH2:45][CH2:46][CH2:47][CH3:48].[CH:21]([Li:22])([CH2:23][CH3:24])[CH3:25].[Cl:1][c:2]1[c:3]2[c:4]([n:5][cH:6][cH:7]1)[n:8]([Si:11]([CH:12]([CH3:13])[CH3:14])([CH:15]([CH3:16])[CH3:17])[CH:18]([CH3:19])[CH3:20])[cH:9][cH:10]2.[O:38]1[CH2:39][CH2:40][CH2:41][CH2:42]1>>[Cl:1][c:2]1[c:3]2[c:4]([n:5][cH:6][c:7]1[C:36]#[N:37])[n:8]([Si:11]([CH:12]([CH3:13])[CH3:14])([CH:15]([CH3:16])[CH3:17])[CH:18]([CH3:19])[CH3:20])[cH:9][cH:10]2

Participants

6

Reactant 5

HCID 8028TetrahydrofuranHCID 8058HexaneHCID 87946p-Toluenesulphonyl cyanideHCID 114382724-Chloro-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridineHCID 178418400CID 53628100

Product 1

HCID 49758988HCID 49758988, compound

Sources & evidence

ORD record
ord-c018fa0bb8ee4d4cae2097c3b44fb844
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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