Phosphorus sulfide (P2S5) → 2-Methyl-8-cyano-5,6,7,8-tetrahydroquinoline

HRID 596476Notes

Reaction equation

HRID 596476 reaction equation
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[CH2:8][CH2:7][CH2:6][CH:5]([C:12]([NH2:14])=O)[C:4]=2[N:3]=1.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=S>>[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[CH2:8][CH2:7][CH2:6][CH:5]([C:12]#[N:14])[C:4]=2[N:3]=1

Participants

3

Reactant 2

HCID 14817Phosphorus sulfide (P2S5)HCID 122789682-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamide

Product 1

HCID 203584122-Methyl-8-cyano-5,6,7,8-tetrahydroquinoline

Procedure

2-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamide was treated with P2S5 to give 2-methyl-8-cyano-5,6,7,8-tetrahydroquinoline which was treated with H2S (both reactions being carried out by a method described in Example 8 to give the title compound as colourless needles from ethylacetate (28%) m.p. 98° (Found: C, 64.32; H, 6.93; N, 13.52%, C11H14N2S requires: C, 64.04; H, 6.84; N, 13.58%).

Sources & evidence

ORD record
ord-7a6e43fd4e6847b9845e744160d9b702
Source dataset
uspto-grants-1977_03
Patent number
US04011225

Reaction notes

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