反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[C:4]([NH2:9])[CH:3]=1.[N:10]([CH:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:16][CH2:15][CH2:14]1)=[C:11]=S>>[F:1][C:2]1[CH:7]=[CH:6][C:5]2[N:8]=[C:11]([NH:10][CH:13]3[C:22]4[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=4)[CH2:16][CH2:15][CH2:14]3)[NH:9][C:4]=2[CH:3]=1参加物
3
実験手順
The title compound was prepared from 4-fluorophenylenediamine and 1-isothiocyanato-1,2,3,4-tetrahydronaphthalene by Procedure D. The title compound was isolated by column chromatography as the free base and as a mixture of enantiomers (solid, mp 220-221° C.). MS(ES+) m/z 282 ([M+1]+, 100).
出典と根拠
- ORDレコード
- ord-b9d79720df6a4456b06914d23a4f9fdc
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07737167B2
関連ノート
読み込み中…