Sodium Azide → 3-Dipropylamino-5-azidochroman

HRID 2257311Notes

Reaction equation

HRID 2257311 reaction equation
[CH2:1]([N:4]([CH2:16][CH2:17][CH3:18])[CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2[NH2:15])[O:7][CH2:6]1)[CH2:2][CH3:3].[N-:19]=[N+:20]=[N-].[Na+]>O>[CH2:16]([N:4]([CH2:1][CH2:2][CH3:3])[CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2[N:15]=[N+:19]=[N-:20])[O:7][CH2:6]1)[CH2:17][CH3:18]

Participants

4

Procedure

3-Dipropylamino-5-aminochroman (Example 14; 0.050 g, 0.20 mmol) was diazotized according to the procedure of Example 15. After stirring for 15 minutes, sodium azide (0.026 g, 0.4 mmol) in water (1.0 ml) was added. After stirring at 5° C. overninght the solution was worked-up and purified according to the procedure of Example 15 to give the title compound. Mp 167°-168° C. (oxalate).

Workup

  1. stirringAfter stirring at 5° C. overninght the solution
  2. custompurified

Sources & evidence

ORD record
ord-41cc1866775e49748f036161b77d949e
Source dataset
uspto-grants-1997_08
Patent number
US05656657

Reaction notes

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