Potassium Cation → HCID 86640045, compound

HRID 2138052Notes

Reaction equation

HRID 2138052 reaction equation
[C:28](=[O:29])([O-:30])[O-:31].[CH3:1][c:2]1[n:3][n:4][c:5](-[c:7]2[cH:8][cH:9][c:10]3[c:11]([c:12](-[c:15]4[cH:16][cH:17][c:18]([OH:21])[cH:19][cH:20]4)[cH:13][o:14]3)[cH:22]2)[o:6]1.[CH3:23][S:24]([Cl:25])(=[O:26])=[O:27].[CH3:34][N:35]([CH3:36])[CH:37]=[O:38].[CH3:39][CH2:40][O:41][C:42](=[O:43])[CH3:44].[K+:32].[K+:33]>>[CH3:1][c:2]1[n:3][n:4][c:5](-[c:7]2[cH:8][cH:9][c:10]3[c:11]([c:12](-[c:15]4[cH:16][cH:17][c:18]([O:21][S:24]([CH3:23])(=[O:26])=[O:27])[cH:19][cH:20]4)[cH:13][o:14]3)[cH:22]2)[o:6]1

Participants

7

Reactant 6

HCID 813Potassium Cation2×HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 31297Methanesulfonyl chlorideHCID 444820244-[5-(5-Methyl-1,3,4-oxadiazol-2-yl)-1-benzofuran-3-yl]phenol

Product 1

HCID 86640045HCID 86640045, compound

Sources & evidence

ORD record
ord-cd96a68486b9431cb398835fcefd8927
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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