Sodium Nitrite → 6,7,8,9-tetrahydro-3H-benzo[1,2-b]1,2,3-triazino[4,5-d]selenophen-4-one

HRID 1097228Notes

Reaction equation

HRID 1097228 reaction equation
[NH2:1][C:2]1[C:3]2[CH2:13][CH2:12][CH2:11][CH2:10][C:4]=2[Se:5][C:6]=1[C:7]([NH2:9])=[O:8].[N:14]([O-])=O.[Na+]>S(=O)(=O)(O)O>[N:1]1[C:2]2[C:3]3[CH2:13][CH2:12][CH2:11][CH2:10][C:4]=3[Se:5][C:6]=2[C:7](=[O:8])[NH:9][N:14]=1

Participants

4

Conditions

Temperature
0 °C

Procedure

To an ice cold (0° C.) solution of 3-amino-4,5,6,7-tetrahydrobenzo[1,2-b]selenophene-2-carboxamide (1.4 g, 5.73 mmol) in concentrated sulfuric acid (10 mL) was added a cold (0° C.) solution of sodium nitrite (0.43 g, 6.31 mmol) in concentrated sulfuric acid (3 mL) for 10 min (while adding, the temperature should keep between −5-0° C.). After addition, the mixture was stirred at 0° C. for 2 h. The reaction mixture was poured into crushed ice slowly with stirring for 15 min and stirred at the same temperature for 15 min. The solution was extracted with ethyl acetate (3×100 mL) and the combined EtOAc layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent to give the product as a pale brown color solid (450 mg, 31%), mp 150-152° C. 1H NMR (400 MHz, DMSO-d6): δ 15.13 (1H, br s, —NH), 3.01-3.04 (2H, m, H-9), 2.90-2.92 (2H, m, H-6), 1.89-1.96 (4H, m, H-7,8); LC-MS (negative ion mode): m/z 252, 254 (M−H)−.

Workup

  1. additionwhile adding
  2. customshould keep between −5-0° C.
  3. additionAfter addition
  4. additionThe reaction mixture was poured
  5. custominto crushed ice slowly
  6. stirringwith stirring for 15 min
  7. stirringstirred at the same temperature for 15 min
  8. extractionThe solution was extracted with ethyl acetate (3×100 mL)
  9. washthe combined EtOAc layer was washed with water, brine
  10. dry with materialdried over sodium sulfate
  11. filtrationThe solution was filtered
  12. customevaporated the solvent

Sources & evidence

ORD record
ord-0290e595fcac4c8d88c6e9fecdee5f73
Source dataset
uspto-grants-2012_03
Patent number
US08143237B2

Reaction notes

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