Oxalyl chloride → HCID 54517899, compound

HRID 1463707Notes

Reaction equation

C(Cl)(=O)[C:2](Cl)=[O:3].[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][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])[C:21]([CH3:37])([CH3:36])[CH2:20]2)[N:11]=[C:10]([NH:38][CH2:39][CH2:40][CH2:41][CH2:42][CH:43]2[CH2:48][C:47]([CH3:50])([CH3:49])[N:46]([O:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH3:59])[C:45]([CH3:61])([CH3:60])[CH2:44]2)[N:9]=1>>[CH2:28]([O:27][N:22]1[C:23]([CH3:26])([CH3:25])[CH2:24][CH:19]([CH2:18][CH2:17][CH2:16][CH2:15][NH:14][C:12]2[N:11]=[C:10]([NH:38][CH2:39][CH2:40][CH2:41][CH2:42][CH:43]3[CH2:44][C:45]([CH3:60])([CH3:61])[N:46]([O:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH3:59])[C:47]([CH3:49])([CH3:50])[CH2:48]3)[N:9]=[C:8]([N:7]=[C:2]=[O:3])[N:13]=2)[CH2:20][C:21]1([CH3:36])[CH3:37])[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35]

Participants

Reactant 2

HCID 65578Oxalyl chloride

HCID 54426568HCID 54426568, compound

Product 1

HCID 54517899HCID 54517899, compound

Procedure

The title compound is prepared from the reaction of oxalyl chloride with the compound prepared in Example 21.

Sources & evidence

ORD record: ord-c040c7c049d64742bc1984ae82f2bc5f
Source dataset: uspto-grants-1994_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05300544

Reaction notes

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