4-Methylpyrazole → HCID 23659708, compound

HRID 1215461Notes

Reaction equation

HRID 1215461 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[n:6][c:7]2[c:8]([n:9]1[CH2:10][CH:11]1[CH2:12][CH2:13][O:14][CH2:15][CH2:16]1)[cH:17][cH:18][c:19]([S:21](=[O:22])(=[O:23])[Cl:24])[cH:20]2.[CH3:25][c:26]1[cH:27][n:28][nH:29][cH:30]1.[CH3:31][N:32]([c:33]1[cH:34][cH:35][n:36][cH:37][cH:38]1)[CH3:39].[CH3:40][C:41]#[N:42]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[n:6][c:7]2[c:8]([n:9]1[CH2:10][CH:11]1[CH2:12][CH2:13][O:14][CH2:15][CH2:16]1)[cH:17][cH:18][c:19]([S:21](=[O:22])(=[O:23])[n:28]1[cH:27][c:26]([CH3:25])[cH:30][n:29]1)[cH:20]2

Participants

5

Reactant 4

HCID 34064-MethylpyrazoleHCID 6342AcetonitrileHCID 142844-(Dimethylamino)pyridineHCID 579372982-tert-Butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazole-5-sulfonyl chloride

Product 1

HCID 23659708HCID 23659708, compound

Sources & evidence

ORD record
ord-8f310621172e4c588090faae78e1ccda
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)

Reaction notes

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