Dimethylformamide → HCID 21992727, compound

HRID 1206322Notes

Reaction equation

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

Participants

Reactant 4

HCID 6228Dimethylformamide

HCID 6344Dichloromethane

HCID 65578Oxalyl chloride

HCID 21992686[4-(2-Pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinolin-7-yloxy]-acetic acid

Product 1

HCID 21992727HCID 21992727, compound

Sources & evidence

ORD record: ord-c6b201e4112346b8a7471bdd6dc9c3cc
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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