2,6-Di-tert-butyl-4-methylpyridine → HCID 178454380, compound

HRID 1126718Notes

Reaction equation

HRID 1126718 reaction equation
[C:26]([c:27]1[cH:28][c:29]([CH3:30])[cH:31][c:32]([C:33]([CH3:34])([CH3:35])[CH3:36])[n:37]1)([CH3:38])([CH3:39])[CH3:40].[CH:1]1([NH:10][c:11]2[cH:12][c:13]([NH:17][CH:18]3[CH2:19][CH:20]([CH2:24][OH:25])[CH:21]([OH:23])[CH2:22]3)[n:14][cH:15][n:16]2)[CH2:2][CH2:3][c:4]2[cH:5][cH:6][cH:7][cH:8][c:9]21.[Cl:41][S:42](=[O:43])(=[O:44])[NH:45][C:46]([O:47][C:48]([CH3:49])([CH3:50])[CH3:51])=[O:52]>>[CH:1]1([NH:10][c:11]2[cH:12][c:13]([NH:17][CH:18]3[CH2:19][CH:20]([CH2:24][O:25][S:42](=[O:43])(=[O:44])[NH:45][C:46]([O:47][C:48]([CH3:49])([CH3:50])[CH3:51])=[O:52])[CH:21]([OH:23])[CH2:22]3)[n:14][cH:15][n:16]2)[CH2:2][CH2:3][c:4]2[cH:5][cH:6][cH:7][cH:8][c:9]21

Participants

4

Reactant 3

HCID 988982,6-Di-tert-butyl-4-methylpyridineHCID 15677406tert-butyl N-(chlorosulfonyl)carbamateHCID 684240234-[[6-(2,3-dihydro-1H-inden-1-ylamino)pyrimidin-4-yl]amino]-2-(hydroxymethyl)cyclopentan-1-ol

Product 1

HCID 178454380HCID 178454380, compound

Sources & evidence

ORD record
ord-75289426c0a74993a56932101471c19f
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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