Oxalyl chloride → HCID 53645908, compound

HRID 1561324Notes

Reaction equation

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

Participants

Reactant 2

HCID 65578Oxalyl chloride

HCID 54289188HCID 54289188, compound

Product 1

HCID 53645908HCID 53645908, compound

Sources & evidence

ORD record: ord-5a22948e492a4defbc6bd89c93c79dcd
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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