Pivaloyl chloride → HCID 72403700, compound

HRID 2131613Notes

Reaction equation

HRID 2131613 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](=[O:15])[C:16]3([NH2:21])[CH2:17][CH2:18][CH2:19][CH2:20]3)[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](=[O:15])[C:16]3([NH:21][C:44]([C:43]([CH3:42])([CH3:47])[CH3:48])=[O:45])[CH2:17][CH2:18][CH2:19][CH2:20]3)[CH2:12][CH2:13]2)[cH:5][cH:6][cH:7]1

Participants

4

Reactant 3

HCID 62493Pivaloyl chlorideHCID 81531DiisopropylethylamineHCID 77537635HCID 77537635, compound

Product 1

HCID 72403700HCID 72403700, compound

Sources & evidence

ORD record
ord-63269ee72cb34ec7b1fb27119fcaf3f0
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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