Phosphorus sulfide (P2S5) → 8-Quinolinecarbothioamide, 2-(1,1-dimethylethyl)-5,6,7,8-tetrahydro-
Reaction equation
[C:1]([C:5]1[CH:14]=[CH:13][C:12]2[CH2:11][CH2:10][CH2:9][CH:8]([C:15]([NH2:17])=O)[C:7]=2[N:6]=1)([CH3:4])([CH3:3])[CH3:2].P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:19]>>[C:1]([C:5]1[CH:14]=[CH:13][C:12]2[CH2:11][CH2:10][CH2:9][CH:8]([C:15](=[S:19])[NH2:17])[C:7]=2[N:6]=1)([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
The title compound was prepared from 2-t-butyl-5,6,7,8-tetrahydroquinoline-8-carboxamide (4 g.) and P2S5 (3 g.) as described in Example 8 and was isolated as creamy needles after recrystallisation from n-hexane m.p. 126° C (650 mgs.). Found: C, 68.18; H, 8.25; N, 11.14%. C14H20N2S requires C, 67.70; H, 8.12; N, 11.23%.
Workup
- customwas isolated as creamy needles
- customafter recrystallisation from n-hexane m.p. 126° C (650 mgs.)
Sources & evidence
- ORD record
- ord-519215d3e69e4c02806a306e401d4280
- Source dataset
- uspto-grants-1978_04
- Patent number
- US04085215
Reaction notes
Loading…