Diethylamine → HCID 19895647, compound

HRID 2140567Notes

Reaction equation

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

Participants

Reactant 6

HCID 8021Diethylamine

HCID 11776Triphenylphosphine

HCID 24290Palladium Chloride

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)

HCID 707143-Iodopyridine

HCID 27790724-[(2-Methylbut-3-yn-2-yl)oxy]benzonitrile

Product 1

HCID 19895647HCID 19895647, compound

Sources & evidence

ORD record: ord-b1f7d2da43644fe28fc89db145935896
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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