Hydrochloric Acid → HCID 178515286, compound

HRID 904569Notes

Reaction equation

HRID 904569 reaction equation
[O:1]=[C:2]1[N:7]2[CH:8]=[C:9]([C:12]#[N:13])[CH:10]=[CH:11][C:6]2=[N:5][C:4]2[CH:14]=[CH:15][S:16][C:3]1=2.[N-:17]=[N+:18]=[N-:19].[Na+].[Cl-].[NH4+].Cl>CN(C)C=O>[NH:17]1[C:12]([C:9]2[CH:10]=[CH:11][C:6]3[N:7]([CH:8]=2)[C:2](=[O:1])[C:3]2[S:16][CH:15]=[CH:14][C:4]=2[N:5]=3)=[N:13][N:19]=[N:18]1

Participants

6

Procedure

A mixture of 10-oxo-10H-pyrido[1,2-a]thieno[3,2-d]pyrimidine-7-carbonitrile (0.6 g., 0.0026 mol), sodium azide (0.56 g., 0.0086 mol) and ammonium chloride (0.46 g., 0.0036 mol) in dimethylformamide (75 ml) is heated at 100°-105° C. for 18 hours under nitrogen. The reaction mixture is cooled, poured into ice water (700 ml) and acidified with concentrated hydrochloric acid (1 ml). The precipitate is filtered off, washed with water, with acetone and dried. Recrystallization from dimethylformamide gives a crystalline product (0.39 g.) mp 300° C. (dec).

Workup

  1. temperatureis heated at 100°-105° C. for 18 hours under nitrogen
  2. temperatureThe reaction mixture is cooled
  3. filtrationThe precipitate is filtered off
  4. washwashed with water, with acetone
  5. customdried
  6. customRecrystallization from dimethylformamide
  7. customgives a crystalline product (0.39 g.) mp 300° C. (dec)

Sources & evidence

ORD record
ord-495b9ac3df394b3b8a90b7f030920b19
Source dataset
uspto-grants-1980_10
Patent number
US04230707

Reaction notes

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