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

HCID 10265300, compound → HCID 53715147, compound

HRID 442753
Notes
Print preview

Reaction equation

HRID 442753 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:10][S:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)(=[O:13])=[O:12])[CH:8]=2)[CH:3]=[CH:2]1.[CH3:20]N1C2C(=CC=C(SC)C=2)C=C1.CSC1C=C2C(C=CN2)=CC=1>>[CH3:20][N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:10][S:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)(=[O:12])=[O:13])[CH:8]=2)[CH:3]=[CH:2]1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 10265300HCID 10265300, compoundHCID 198489176-(Methylsulfanyl)-1H-indoleHCID 539966581-Methyl-6-(methylthio)-1H-indole

Product 1

HCID 53715147HCID 53715147, compound

Procedure

Benzenesulfonic acid 1-methyl-1H-indol-6-yl ester was prepared from the known benzenesulfonic acid 1-H-indol-6-yl ester according to the procedure described above for the preparation of 1-methyl-6-methylsulfanyl-1H-indole from 6-methylsulfanyl-1H-indole.

Sources & evidence

ORD record
ord-0835082a93944c07af551b5eb7608acf
Source dataset
On this pageParticipantsProcedureSources & evidenceReaction notes
uspto-grants-1999_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05891901

Reaction notes

Loading…