反応式
N[C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][CH:3]=1.C(Cl)(Cl)=S.C(OC(C1C=CC([N:28]=[C:29]=[S:30])=CC=1)=O)C.NN.C(OC(C1C=CC([NH:44][NH:45]C(N)=S)=CC=1)=O)C.Cl.[N:50]([O-])=O.[Na+]>C(Cl)(Cl)Cl.O.C(O)C>[CH2:9]([O:8][C:6]([C:5]1[CH:11]=[CH:12][C:2]([C:29]2[SH:30]([NH2:50])[N:45]=[N:44][N:28]=2)=[CH:3][CH:4]=1)=[O:7])[CH3:10]参加物
反応物 7
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- 5 °C
実験手順
0.1 Mol of ethyl p-aminobenzoate was mixed with 150 ml of water and stirred for 15 minutes. Thiophosgene (10 g) in 50 ml chloroform was added dropwise. The mixture was stirred for 2 hours at 15° C. The organic solution was washed with HCl 2N, dried and the solvent was removed under vacuum to obtain a yellow-red oil, that was used as crude product. 0.02 mMole of the obtained 4-ethoxycarbonylphenylisothiocyanate and 30 ml ethanol were stirred in a flask and added dropwise with 2 ml 85% hydrazine in 2 ml water. After 15 minutes the crude product separated and was filtered under vacuum. Yield 90%. 0.01 Mole of the obtained 4-ethoxycarbonylphenylthiosemicarbazide was mixed with a solution of 1.5 ml HCl 37% and 35 ml water. The mixture was cooled to 5° C. and 0.8 g sodium nitrite dissolved in 5 ml water was added dropwise. The mixture was stirred for 30 minutes at 5° C. The crude product was filtered, washed with water and dried. Yield 80%. The product was crystallized from methanol. The structure was confirmed by IR and NMR spectroscopy.
後処理
- stirringThe mixture was stirred for 2 hours at 15° C
- washThe organic solution was washed with HCl 2N
- customdried
- customthe solvent was removed under vacuum
- customto obtain a yellow-red oil, that
- customAfter 15 minutes the crude product separated
- filtrationwas filtered under vacuum
- additionwas added dropwise
- stirringThe mixture was stirred for 30 minutes at 5° C
- filtrationThe crude product was filtered
- washwashed with water
- customdried
- customThe product was crystallized from methanol
出典と根拠
- ORDレコード
- ord-6bb0f49f7b484b7d9fc48c25f6532664
- 出典データセット
- uspto-grants-1993_08
- 特許番号
- US05232826
関連ノート
読み込み中…