Pivaloyl chloride → HCID 72403767, compound

HRID 1562322Notes

Reaction equation

HRID 1562322 reaction equation
[CH3:42][C:43]([C:44](=[O:45])[Cl:46])([CH3:47])[CH3:48].[CH:49]([N:50]([CH2:51][CH3:52])[CH:53]([CH3:54])[CH3:55])([CH3:56])[CH3:57].[F:1][c:2]1[cH:3][c:4]([C:8]2([CH2:22][CH2:23][N:24]3[CH:25]4[CH2:26][CH:27]([n:32]5[c:33]([CH3:41])[n:34][c:35]6[c:36]5[cH:37][cH:38][cH:39][cH:40]6)[CH2:28][CH:29]3[CH2:30][CH2:31]4)[CH2:9][CH2:10][N:11]([C:14]([C:15]([CH:16]([CH3:17])[CH3:18])([NH2:19])[CH3:20])=[O:21])[CH2:12][CH2:13]2)[cH:5][cH:6][cH:7]1>>[F:1][c:2]1[cH:3][c:4]([C:8]2([CH2:22][CH2:23][N:24]3[CH:25]4[CH2:26][CH:27]([n:32]5[c:33]([CH3:41])[n:34][c:35]6[c:36]5[cH:37][cH:38][cH:39][cH:40]6)[CH2:28][CH:29]3[CH2:30][CH2:31]4)[CH2:9][CH2:10][N:11]([C:14]([C:15]([CH:16]([CH3:17])[CH3:18])([NH:19][C:44]([C:43]([CH3:42])([CH3:47])[CH3:48])=[O:45])[CH3:20])=[O:21])[CH2:12][CH2:13]2)[cH:5][cH:6][cH:7]1

Participants

4

Reactant 3

HCID 62493Pivaloyl chlorideHCID 81531DiisopropylethylamineHCID 77537897HCID 77537897, compound

Product 1

HCID 72403767HCID 72403767, compound

Sources & evidence

ORD record
ord-51812f2fe2fd492bb621de8fb7e854e5
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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