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

4-Methoxy-3-(trifluoromethyl)benzyl bromide → 6-[5-[[4-Methoxy-3-(trifluoromethyl)benzyl]thio]-1,3,4-oxadiazol-2-yl]quinoline

HRID 452752
Notes
Print preview

Reaction equation

HRID 452752 reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][C:7]([C:11]3[O:15][C:14]([SH:16])=[N:13][N:12]=3)=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[CH3:17][O:18][C:19]1[CH:26]=[CH:25][C:22]([CH2:23]Br)=[CH:21][C:20]=1[C:27]([F:30])([F:29])[F:28]>>[CH3:17][O:18][C:19]1[CH:26]=[CH:25][C:22]([CH2:23][S:16][C:14]2[O:15][C:11]([C:7]3[CH:6]=[C:5]4[C:10](=[CH:9][CH:8]=3)[N:1]=[CH:2][CH:3]=[CH:4]4)=[N:12][N:13]=2)=[CH:21][C:20]=1[C:27]([F:28])([F:30])[F:29]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 27753024-Methoxy-3-(trifluoromethyl)benzyl bromideHCID 1785279365-(6-Quinolyl)-1,3,4-oxadiazole-2-thiol

Product 1

HCID 445904656-[5-[[4-Methoxy-3-(trifluoromethyl)benzyl]thio]-1,3,4-oxadiazol-2-yl]quinolineYield 74%

Procedure

In the same manner as in Example 7 and using 5-(6-quinolyl)-1,3,4-oxadiazole-2-thiol instead of 5-(1H-indazol-5-yl)-1,3,4-oxadiazole-2-thiol and 4-methoxy-3-(trifluoromethyl)benzyl bromide instead of 3-(trifluoromethyl)benzyl chloride, the title compound (yield 74%) was obtained as colorless crystals.

Sources & evidence

ORD record
ord-75b00fcfe11b45d583afbfe00838f336
Source dataset
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08492378B2

Reaction notes

Loading…

On this pageParticipantsProcedureSources & evidenceReaction notes