Hydrochloric Acid → HCID 178432027, compound

HRID 649153Notes

Reaction equation

HRID 649153 reaction equation
[C:1]([CH2:3][C:4]1[N:8]2[CH:9]=[CH:10][C:11]3[C:16]([C:7]2=[N:6][C:5]=1[CH3:17])=[CH:15][CH:14]=[CH:13][CH:12]=3)#[N:2].[Cl-].[NH4+].[N-:20]=[N+:21]=[N-:22].[Na+].Cl.C(=O)(O)[O-].[Na+]>CN(C)C=O.O>[CH3:17][C:5]1[N:6]=[C:7]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[CH:10]=[CH:9][N:8]2[C:4]=1[CH2:3][C:1]1[NH:22][N:21]=[N:20][N:2]=1

Participants

8

Procedure

A mixture of 3-cyanomethyl-2-methylimidazo[2,1-a]isoquinoline (2.8 g), ammonium chloride (0.74 g) and sodium azide (0.9 g) in N,N-dimethylformamide (28 ml) was heated at 120°-125° C. with stirring for 18 hours. The solution was poured into water, acidified with concentrated hydrochloric acid and then neutralized with an aqueous solution of sodium bicarbonate. The resulting precipitates were collected by filtration, washed with water and recrystallized from a mixture of chloroform and methanol to give 2-methyl-3-[(1H-tetrazol-5-yl)methyl]imidazo[2,1-a]isoquinoline (2.9 g).

Workup

  1. temperaturewas heated at 120°-125° C.
  2. customThe resulting precipitates
  3. filtrationwere collected by filtration
  4. washwashed with water
  5. customrecrystallized from a mixture of chloroform and methanol

Sources & evidence

ORD record
ord-16311fe578044c579d4bae41928e0571
Source dataset
uspto-grants-1988_04
Patent number
US04738967

Reaction notes

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