Bromide ion → HCID 16037645, compound

HRID 700528Notes

Reaction equation

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

Participants

Reactant 7

HCID 259Bromide ion

HCID 813Potassium Cation2×

HCID 8028Tetrahydrofuran

HCID 19660Carbonate Ion

HCID 83681Tris(1,1-dimethylethyl)phosphine

HCID 11708078(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acid

HCID 71423725(4-Bromo-2-methoxyphenyl)cyanamide

Product 1

HCID 16037645HCID 16037645, compound

Sources & evidence

ORD record: ord-014801f1b6504347b8aac061417f5fc1
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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