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

5-Chloropyrazinoic acid → 5-(Oxetan-2-ylmethoxy)pyrazine-2-carboxylic acid

HRID 571744
Notes
Print preview

Reaction equation

HRID 571744 reaction equation
Cl[C:2]1[N:3]=[CH:4][C:5]([C:8]([OH:10])=[O:9])=[N:6][CH:7]=1.[O:11]1[CH2:14][CH2:13][CH:12]1[CH2:15][OH:16].CC(C)([O-])C.[K+]>CN(C)C=O>[O:11]1[CH2:14][CH2:13][CH:12]1[CH2:15][O:16][C:2]1[N:3]=[CH:4][C:5]([C:8]([OH:10])=[O:9])=[N:6][CH:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 4654725-Chloropyrazinoic acidHCID 12284142(Oxetan-2-yl)methanolHCID 23665647Potassium tert-butoxide

Product 1

HCID 1177383715-(Oxetan-2-ylmethoxy)pyrazine-2-carboxylic acidYield 221.7%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
120 °C

Procedure

In a microwave vial 5-chloropyrazine-2-carboxylic acid (100.0 mg, 0.631 mmol), dimethylformamide (5 mL), oxetan-2-ylmethanol (83.4 mg, 0.946 mmol) and potassium tert-butoxide (176.9 mg, 1.58 mmol) are added. A small exotherm is observed. After 1 minute at room temperature the vial is sealed and the mixture heated at 120° C. for 30 minutes in the microwave. The reaction mixture is then quenched with aqueous NH4Cl and the solvent evaporated under reduced pressure. The resultant residue is triturated in 2-propanol. The filtrate is concentrated under reduced pressure to give the title compound as a cream solid (0.294 g, 99%) and is used without further purification. ES/MS (m/e): 211.0 (M+1), 208.8 (M−H).

Workup

  1. customAfter 1 minute at room temperature the vial is sealed
  2. customThe reaction mixture is then quenched with aqueous NH4Cl
  3. customthe solvent evaporated under reduced pressure
  4. customThe resultant residue is triturated in 2-propanol
  5. concentrationThe filtrate is concentrated under reduced pressure

Sources & evidence

ORD record
ord-5e8954cb5c7647bbb4d1d8c8501e4832
Source dataset
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09029367B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes