反応式
[NH2:1][C:2]1[C:6]([NH2:7])=[CH:5][S:4][CH:3]=1.C(N(CC)CC)C.[C:15](Cl)(=[O:20])[CH2:16][CH2:17][CH2:18][CH3:19]>C(Cl)Cl>[NH2:1][C:2]1[C:6]([NH:7][C:15](=[O:20])[CH2:16][CH2:17][CH2:18][CH3:19])=[CH:5][S:4][CH:3]=1参加物
5
実験手順
3.06 g of 3,4-diaminothiophene were mixed with 45 ml of methylene chloride and 9 ml of triethylamine and a solution of 3.6 g of valeroyl chloride in 45 ml of methylene chloride was added at a temperature of 20° C. over one hour. The mixture was stirred for 30 minutes, followed by evaporation to dryness. After separation by chromatography (eluant: methanol/methylene chloride 5/95), 3.2 g of the expected monoamide were obtained which was crystallized from 15 ml of a 50/50 mixture of isopropyl ether and cyclohexane. The crystals were separated, washed with this mixture and dried under reduced pressure at 100° C. to obtain 2.14 g of the expected product melting at 110° C.
後処理
- customfollowed by evaporation to dryness
- customAfter separation by chromatography (eluant: methanol/methylene chloride 5/95), 3.2 g of the expected monoamide
- customwere obtained which
- customwas crystallized from 15 ml of a 50/50 mixture of isopropyl ether and cyclohexane
- customThe crystals were separated
- washwashed with this mixture
- customdried under reduced pressure at 100° C.
出典と根拠
- ORDレコード
- ord-6e5bfdb6288e4302b1e9238335883240
- 出典データセット
- uspto-grants-1995_02
- 特許番号
- US05389634
関連ノート
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