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

Hydrochloric Acid → 2-Chloro-6-fluoro-5-methoxy-1,3-benzothiazole

HRID 2368096
Notes
Print preview

Reaction equation

HRID 2368096 reaction equation
N(OC(C)(C)C)=O.[F:8][C:9]1[C:18]([O:19][CH3:20])=[CH:17][C:12]2[N:13]=[C:14](N)[S:15][C:11]=2[CH:10]=1.[ClH:21]>C(#N)C.[Cl-].[Na+].O.[Cu](Cl)Cl>[Cl:21][C:14]1[S:15][C:11]2[CH:10]=[C:9]([F:8])[C:18]([O:19][CH3:20])=[CH:17][C:12]=2[N:13]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 313Hydrochloric AcidHCID 10906Tert-Butyl nitriteHCID 57517493HCID 57517493, compound

Product 1

HCID 575174942-Chloro-6-fluoro-5-methoxy-1,3-benzothiazole

Reagents, catalysts & solvents 3

HCID 24014Cupric ChlorideCatalystHCID 6342Acetonitrile
Solvent
2×
HCID 57417360Sodium chloride; waterSolvent

Conditions

Temperature
50 °C

Procedure

A suspension of copper(II) chloride (546 mg) and tert-butyl nitrite (0.600 mL) in acetonitrile (10 mL) was stirred at 50° C. for 20 min. To the reaction mixture was added a solution of 6-fluoro-5-methoxy-1,3-benzothiazol-2-amine (670 mg) in acetonitrile (10 mL), and the mixture was further stirred at 50° C. for 30 min. 1M Hydrochloric acid and saturated brine were added to the reaction mixture, and the insoluble material was filtered. The filtrate was extracted with ethyl acetate, the filtered insoluble material was dissolved in THF, and the solution was combined with the organic layer. The mixture was applied to silica gel column chromatography (ethyl acetate). The solvent was evaporated under reduced pressure and the obtained solid was washed with ethyl acetate/hexane to give the title compound (350 mg).

Workup

  1. stirringthe mixture was further stirred at 50° C. for 30 min
  2. filtrationthe insoluble material was filtered
  3. extractionThe filtrate was extracted with ethyl acetate
  4. dissolutionthe filtered insoluble material was dissolved in THF
  5. customThe solvent was evaporated under reduced pressure
  6. washthe obtained solid was washed with ethyl acetate/hexane

Sources & evidence

ORD record
ord-c3eca9da52ee4295828810fab096eaa5
Source dataset
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08703758B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes