Hydrogen Sulfide → HCID 20443839, compound
Reaction equation
[C:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]2[O:10][CH2:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[C:5]=2[CH:4]=1)#[N:2].N1C=CC=CC=1.[SH2:24]>C(N(CC)CC)C>[CH:4]1[C:5]2[C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=3[CH2:11][O:10][C:6]=2[NH:7][C:8](=[O:9])[C:3]=1[C:1](=[S:24])[NH2:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Add 4.20 gm of 2-cyano-4,6-dihydro-3H[2]benzopyrano[3,4-b]-pyridin-3-one to 50 gm of pyridine. Add 3.0 ml of triethylamine to the system. Cool the system to 0°-5° and treat the system with hydrogen sulfide gas until the reaction is complete as indicated by thin layer chromatography. Isolate the title compound.
Workup
- temperatureCool the system to 0°-5°
Sources & evidence
- ORD record
- ord-bd6bdbbb1de245d284eb04ca648d569d
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04474786
Reaction notes
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