Oxalyl chloride → HCID 54348016, compound

HRID 2144253Notes

Reaction equation

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

Participants

Reactant 2

HCID 65578Oxalyl chloride

HCID 53764606HCID 53764606, compound

Product 1

HCID 54348016HCID 54348016, compound

Sources & evidence

ORD record: ord-5d6b699ed93c4f919a1c9a70c17b3846
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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