Methane → HCID 178435054, compound

HRID 1155903Notes

Reaction equation

HRID 1155903 reaction equation
[CH3:1][C:2]1[S:3][C:4]([CH3:18])=[C:5]2[C:10]=1[C:9](=[O:11])[N:8]1[CH:12]=[C:13]([C:16]#[N:17])[CH:14]=[CH:15][C:7]1=[N:6]2.[N-:19]=[N+:20]=[N-:21].[Na+].[Cl-].[NH4+].C>CN(C)C=O.N1C=CC=CC=1>[CH3:1][C:2]1[S:3][C:4]([CH3:18])=[C:5]2[C:10]=1[C:9](=[O:11])[N:8]1[CH:12]=[C:13]([C:16]3[NH:21][N:20]=[N:19][N:17]=3)[CH:14]=[CH:15][C:7]1=[N:6]2

Participants

7

Conditions

Temperature
120 °C

Procedure

A mixture of 4.4 g (0.0172 mol) of 1,3-dimethyl-10-oxo-10H-pyrido[1,2-a]thieno[3,4-d]pyrimidine-7-carbonitrile (Example 51), 6.5 g (0.1 mol) of sodium azide and 5.3 g (0.1 mol) of ammonium chloride in 180 ml of dimethylformamide is stirred and heated in a wax bath at 120° C. for seventeen hours under nitrogen. The reaction mixture is cooled, filtered and filtrate evaporated. The residue is treated with 250 ml of water and acidified with concentrated hydrochloric acid. This mixture is warmed on a steam bath, cooled and filtered to give 5.1 g of crude product. This material is dissolved in hot pyridine, activated charcoal (Darco-G60, Matheson, Coleman and Bell) is added and the hot suspension is filtered through Supercell Hyflo® (Johns-Mansville). The filtrate is cooled to give 3.1 g of 1,3-dimethyl-7-(1H-tetrazol-5-yl)-10H-pyrido[1,2-a]thieno-[3,4-d]pyrimidin-10-one; mp 292° C. (dec).

Workup

  1. temperatureThe reaction mixture is cooled
  2. filtrationfiltered
  3. customfiltrate evaporated
  4. additionThe residue is treated with 250 ml of water
  5. temperatureThis mixture is warmed on a steam bath
  6. temperaturecooled
  7. filtrationfiltered
  8. customto give 5.1 g of crude product
  9. filtrationthe hot suspension is filtered through Supercell Hyflo® (Johns-Mansville)
  10. temperatureThe filtrate is cooled

Sources & evidence

ORD record
ord-1c9454ddac8748468b878cbcd5fbbf27
Source dataset
uspto-grants-1982_06
Patent number
US04332947

Reaction notes

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