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Potassium Iodide → HCID 18998777, compound

HRID 2260607
Notes
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Reaction equation

HRID 2260607 reaction equation
[I-].[K+].[SH:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH3:14])[C:9](=[O:15])[CH2:8][CH2:7]2.Cl[C:17]1[S:18][C:19]([C:22]2([O:30][CH3:31])[CH2:27][CH2:26][O:25][C:24]([CH3:29])([CH3:28])[CH2:23]2)=[CH:20][N:21]=1>>[CH3:31][O:30][C:22]1([C:19]2[S:18][C:17]([S:3][C:4]3[CH:5]=[C:6]4[C:11](=[CH:12][CH:13]=3)[N:10]([CH3:14])[C:9](=[O:15])[CH2:8][CH2:7]4)=[N:21][CH:20]=2)[CH2:27][CH2:26][O:25][C:24]([CH3:29])([CH3:28])[CH2:23]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 4875Potassium IodideHCID 189987784-(2-Chlorothiazol-5-yl)-4-methoxy-2,2-dimethyltetrahydropyranHCID 224137591-Methyl-6-sulfanyl-1,2,3,4-tetrahydroquinolin-2-one

Product 1

HCID 18998777HCID 18998777, compoundYield 80%

Procedure

Using an analogous procedure to that described in Example 1 except that a catalytic amount (0.01 g) of potassium iodide was added, 6-mercapto-1-methyl-1,2,3,4-tetrahydroquinolin-2-one was reacted with 4-(2-chlorothiazol-5-yl)-4-methoxy-2,2-dimethyltetrahydropyran to give 4-methoxy-2,2-dimethyl-4-[2-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-ylthio)thiazol-5-yl]tetrahydropyran in 80% yield as a foam;

Workup

  1. additionwas added

Sources & evidence

ORD record
ord-4e574e22ff764758bbd5e024e42759d5
Source dataset
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05478843

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes