Acetate → 2-Sulfamoyl-6-benzothiazolyl acetate

HRID 2154476Notes

Reaction equation

HRID 2154476 reaction equation
[C:16]([CH3:17])(=[O:18])[O-:19].[C:37]([O-:38])(=[O:39])[CH3:40].[C:42]([O-:43])(=[O:44])[CH3:45].[CH3:33][C:34](=[O:35])[OH:36].[K+:21].[K+:22].[Li+:20].[O-:23][Cr:24]([O:25][Cr:26](=[O:27])(=[O:28])[O-:29])(=[O:30])=[O:31].[OH2:14].[OH2:15].[OH2:32].[Pd+2:41].[s:1]1[c:2]([S:10](=[O:11])(=[O:12])[NH2:13])[n:3][c:4]2[c:5]1[cH:6][cH:7][cH:8][cH:9]2>>[s:1]1[c:2]([S:10](=[O:11])(=[O:12])[NH2:13])[n:3][c:4]2[c:5]1[cH:6][c:7]([O:19][C:16]([CH3:17])=[O:18])[cH:8][cH:9]2

Participants

9

Reactant 8

HCID 175Acetate3×HCID 176Acetic AcidHCID 813Potassium Cation2×HCID 962Water3×HCID 24503Dichromate ionHCID 28486Lithium ionHCID 679442-BenzothiazolesulfonamideHCID 105144Allyl(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)chloropalladium(II)

Product 1

HCID 132366622-Sulfamoyl-6-benzothiazolyl acetate

Sources & evidence

ORD record
ord-16a89b72311b4238bf6c1320995318a1
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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