Potassium Cation → (3-Amino-5-chloro-2-cyclopropylcarbamoyl-4-methyl-thieno[2,3-b]pyridin-6-yloxy)-acetic acid

Reaktionsgleichung

[CH2:31]1[O:32][CH2:33][CH2:34][CH2:35]1.[CH3:1][O:2][C:3]([CH2:4][O:5][c:6]1[c:7]([Cl:23])[c:8]([CH3:22])[c:9]2[c:10]([n:11]1)[s:12][c:13]([C:16]([NH:17][CH:18]1[CH2:19][CH2:20]1)=[O:21])[c:14]2[NH2:15])=[O:24].[CH3:25][Si:26]([CH3:27])([CH3:28])[O-:29].[K+:30]>>[O:2]=[C:3]([CH2:4][O:5][c:6]1[c:7]([Cl:23])[c:8]([CH3:22])[c:9]2[c:10]([n:11]1)[s:12][c:13]([C:16]([NH:17][CH:18]1[CH2:19][CH2:20]1)=[O:21])[c:14]2[NH2:15])[OH:24]

Komponenten

Edukt 4

HCID 813Potassium Cation

HCID 8028Tetrahydrofuran

HCID 3588738[SIMe3O]-

HCID 68436041(3-Amino-5-chloro-2-cyclopropylcarbamoyl-4-methyl-thieno[2,3-b]pyridin-6-yloxy)-acetic acid methylester

Produkt 1

HCID 68436813(3-Amino-5-chloro-2-cyclopropylcarbamoyl-4-methyl-thieno[2,3-b]pyridin-6-yloxy)-acetic acid

Quellen und Nachweise

ORD-Eintrag: ord-bf83397a6a594037b0b2e9f2c790d3ab
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D

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