HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Potassium Cation → 6,7-Dimethoxy-4-(5-nitrothiophen-2-ylsulfanyl)quinoline

HRID 168817
Notes
Print preview

Reaction equation

HRID 168817 reaction equation
[Br:16][c:17]1[s:18][c:19]([N+:22](=[O:23])[O-:24])[cH:20][cH:21]1.[C:25](=[O:26])([O-:27])[O-:28].[CH3:1][O:2][c:3]1[cH:4][c:5]2[c:6](=[S:15])[cH:7][cH:8][nH:9][c:10]2[cH:11][c:12]1[O:13][CH3:14].[CH3:31][CH2:32][O:33][C:34](=[O:35])[CH3:36].[CH3:37][N:38]([CH3:39])[CH:40]=[O:41].[K+:29].[K+:30].[OH2:42]>>[CH3:1][O:2][c:3]1[cH:4][c:5]2[c:6]([S:15][c:17]3[s:18][c:19]([N+:22](=[O:23])[O-:24])[cH:20][cH:21]3)[cH:7][cH:8][n:9][c:10]2[cH:11][c:12]1[O:13][CH3:14]
ParticipantsSources & evidenceReaction notes

Participants

8

Reactant 7

HCID 813Potassium Cation2×HCID 962WaterHCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 832222-Bromo-5-nitrothiopheneHCID 229368096,7-Dimethoxyquinoline-4(1H)-thione

Product 1

Sources & evidence

ORD record
ord-1374c95cda04457aa43ba48f168f141a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI
10.1039/C8SC04228D

Reaction notes

Loading…

On this pageParticipantsSources & evidenceReaction notes
HCID 229368146,7-Dimethoxy-4-(5-nitrothiophen-2-ylsulfanyl)quinoline