Oxalyl chloride → HCID 54348016, compound

HRID 1463708Notes

Reaction equation

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

Participants

Reactant 2

HCID 65578Oxalyl chloride

HCID 53764606HCID 53764606, compound

Product 1

HCID 54348016HCID 54348016, compound

Procedure

The title compound is prepared from the reaction of oxalyl chloride with the compound prepared in Example 20.

Sources & evidence

ORD record: ord-404c77f3ec3d4981836ee86d7a765f85
Source dataset: uspto-grants-1994_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05300544

Reaction notes

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