HCID 23509742, compound → HCID 178522718, compound

HRID 414454Notes

Reaction equation

HRID 414454 reaction equation
[N:1]1([C:6]2[N:11]=[C:10]([C:12]([OH:14])=O)[CH:9]=[N:8][CH:7]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[NH2:15][C:16]1[NH:20][N:19]=[N:18][N:17]=1>O1CCCC1.C(N(CC)CC)C.C(Cl)(=O)C(C)(C)C>[N:1]1([C:6]2[N:11]=[C:10]([C:12]([NH:15][C:16]3[NH:20][N:19]=[N:18][N:17]=3)=[O:14])[CH:9]=[N:8][CH:7]=2)[CH2:2][CH2:3][CH2:4][CH2:5]1

Participants

6

Procedure

To a suspension of 2.90 g of 6-(1-pyrrolidinyl) pyrazine-2-carboxylic acid in 45 ml of tetrahydrofuran, 2.30 ml of triethylamine and 2.00 ml of pivaloyl chloride were added dropwise successively at 0 ° C. under stirring. After stirring for 1 hour at 0 ° C., 1.40 g of 5-amino-1H-tetrazole was added to the mixture, and the reaction mixture was stirred for 1 hour at room temperature, and then refluxed for 12 hours, The reaction mixture was evaporated, and water was added to the residue. The precipitate was collected by filtration, and recrystalized from dimethylsulfoxide affording 1.63 g of the desired compound as yellow needles. The obtained crystal was consistent with that of (a)

Workup

  1. additionwere added dropwise successively at 0 ° C.
  2. stirringAfter stirring for 1 hour at 0 ° C.
  3. stirringthe reaction mixture was stirred for 1 hour at room temperature
  4. temperaturerefluxed for 12 hours
  5. customThe reaction mixture was evaporated
  6. additionwater was added to the residue
  7. filtrationThe precipitate was collected by filtration
  8. customrecrystalized from dimethylsulfoxide affording 1.63 g of the desired compound as yellow needles

Sources & evidence

ORD record
ord-9011014c3f624c968f4760f8b928526f
Source dataset
uspto-grants-1988_12
Patent number
US04792547

Reaction notes

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