Chloride → HCID 59152218, compound

HRID 282359Notes

Reaction equation

HRID 282359 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[n:5]1[n:6][cH:7][cH:8][c:9]1[NH:10][c:11]1[cH:12][n:13][cH:14][c:15]([CH2:17][OH:18])[n:16]1.[CH3:28][S:29](=[O:30])(=[O:31])[Cl:32].[CH3:39][CH2:40][O:41][C:42](=[O:43])[CH3:44].[CH3:45][N:46]([CH3:47])[CH:48]=[O:49].[CH:19]([N:20]([CH:21]([CH3:22])[CH3:23])[CH2:24][CH3:25])([CH3:26])[CH3:27].[CH:35]([Cl:36])([Cl:37])[Cl:38].[Cl-:34].[Li+:33]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[n:5]1[n:6][cH:7][cH:8][c:9]1[NH:10][c:11]1[cH:12][n:13][cH:14][c:15]([CH2:17][Cl:32])[n:16]1

Participants

9

Reactant 8

HCID 312ChlorideHCID 6212ChloroformHCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 28486Lithium ionHCID 31297Methanesulfonyl chlorideHCID 81531DiisopropylethylamineHCID 59152207{6-[(1-tert-Butyl-1H-pyrazol-5-yl)amino]pyrazin-2-yl}methanol

Product 1

HCID 59152218HCID 59152218, compound

Sources & evidence

ORD record
ord-20586de4547642d0a1bb19d012b4124c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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