Furfurylamine → HCID 12493316, compound
Reaction equation
CS[C:3]1[N:8]2[CH:9]=[CH:10][N:11]=[C:7]2[CH:6]=[N:5][N:4]=1.[CH2:12]([NH2:18])[C:13]1[O:17][CH:16]=[CH:15][CH:14]=1>>[CH2:12]([NH:18][C:3]1[N:8]2[CH:9]=[CH:10][N:11]=[C:7]2[CH:6]=[N:5][N:4]=1)[C:13]1[O:17][CH:16]=[CH:15][CH:14]=1Participants
3
Procedure
A 5.0 gm. portion of 5-(methylthio)-imidazo[1,2-d]-as-triazine is combined with 45 ml. of furfurylamine and refluxed for 2 hours. The mixture is allowed to stand at room temperature overnight. The gummy solid is collected and crystallized from 60 ml. of hot methanol, giving 2.75 gm. of the desired product as crystals, m.p. 212°-214° C.
Workup
- customThe gummy solid is collected
- customcrystallized from 60 ml
- customof hot methanol, giving 2.75 gm
Sources & evidence
- ORD record
- ord-664eda491cf44ff4b2bbf904d8eab2c2
- Source dataset
- uspto-grants-1978_08
- Patent number
- US04107309
Reaction notes
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