Potassium Cation → HCID 11641266, compound

HRID 1233322Notes

Reaction equation

[CH2:36]1[CH2:37][O:38][CH2:39][CH2:40][NH:41]1.[CH3:3][S:4]([O:5][CH2:8][CH2:9][O:10][c:11]1[n:12][nH:13][c:14]2[n:15][cH:16][n:17][c:18]([NH:20][c:21]3[cH:22][c:23]([F:35])[c:24]([O:27][c:28]4[cH:29][n:30][c:31]([CH3:34])[cH:32][cH:33]4)[cH:25][cH:26]3)[c:19]12)(=[O:6])=[O:7].[I-:2].[K+:1]>>[CH2:8]([CH2:9][O:10][c:11]1[n:12][nH:13][c:14]2[n:15][cH:16][n:17][c:18]([NH:20][c:21]3[cH:22][c:23]([F:35])[c:24]([O:27][c:28]4[cH:29][n:30][c:31]([CH3:34])[cH:32][cH:33]4)[cH:25][cH:26]3)[c:19]12)[N:41]1[CH2:36][CH2:37][O:38][CH2:39][CH2:40]1

Participants

Reactant 4

HCID 813Potassium Cation

HCID 8083Morpholine

HCID 30165Iodide Ion

HCID 11719830Ethanol, 2-[[4-[[3-fluoro-4-[(6-methyl-3-pyridinyl)oxy]phenyl]amino]-1H-pyrazolo[3,4-d]pyrimidin-3-yl]oxy]-, 1-methanesulfonate

Product 1

HCID 11641266HCID 11641266, compound

Sources & evidence

ORD record: ord-3a2c70483b4544efbfe1162615237914
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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