Triethylamine → HCID 12451285, compound
Reaction equation
[C:1](Cl)(Cl)=[S:2].[CH3:5][NH:6][N:7]([CH3:17])[C:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:9].C(N(CC)CC)C>C(Cl)(Cl)Cl.ClCCl>[CH3:5][N:6]1[C:1](=[S:2])[N:10]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:8](=[O:9])[N:7]1[CH3:17]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 4.26 g (0.037 mol) thiophosgene in about 10 ml chloroform was added dropwise to a solution of 6.7 g (0.037 mol) 1,2-dimethyl-4-phenylsemicarbazide and 7.47 g (0.074 mol) triethylamine in 200 ml chloroform. A slightly exothermic reaction ensued. One hour after the addition was completed, the reaction mixture was heated under reflux for about 16 hours, cooled and evaporated under reduced pressure to give an oil residue. The residue was dissolved in dichloromethane, washed with water, dried over magnesium sulfate, filtered and evaporated under reduced pressure to give a red viscous oil. The oil was chromatographed on 200 g of silica gel using dichloromethane as eluant. The major product (4 g) from the chromatography was a semisolid, which on trituration with ether gave the desired product as a light tan solid, m.p. 118°-122° C. Infrared spectrum of the product showed strong carbonyl absorption at 5.8 micron. The product is tabulated in Table I as Compound No. 1.
Workup
- customA slightly exothermic reaction
- additionOne hour after the addition
- temperaturethe reaction mixture was heated
- temperatureunder reflux for about 16 hours
- temperaturecooled
- customevaporated under reduced pressure
- customto give an oil residue
- washwashed with water
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated under reduced pressure
- customto give a red viscous oil
- customThe oil was chromatographed on 200 g of silica gel
Sources & evidence
- ORD record
- ord-c82b77f8c4ab430bacab3ada615d0351
- Source dataset
- uspto-grants-1982_04
- Patent number
- US04326878
Reaction notes
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