Ethylenediamine → HCID 13753971, compound
Reaction equation
[NH2:1][C:2]1[C:3]([Cl:14])=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]([C:12]#[N:13])[CH2:7][CH2:6][CH2:5]2.[CH2:15](N)[CH2:16][NH2:17]>>[ClH:14].[NH2:1][C:2]1[C:3]([Cl:14])=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]([C:12]1[NH:17][CH2:16][CH2:15][N:13]=1)[CH2:7][CH2:6][CH2:5]2Participants
3
Procedure
Utilizing the procedure of Example 74 with 6-amino-1-cyano-5-chloro-(1,2,3,4-tetrahydronaphthalene) (1.2 g) and ethylenediamine (3 ml) gave the desired compound in 60% yield. m.p. 220° C. (decomp.).
Sources & evidence
- ORD record
- ord-55038710ea3549b4a24f2e1175141756
- Source dataset
- uspto-grants-1987_01
- Patent number
- US04634705
Reaction notes
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