Acetic Anhydride → HCID 178425986、化合物
反応式
[C:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][N+:9]1[C:17]2[C:12](=[C:13]([F:21])[C:14]([F:20])=[C:15]([F:19])[C:16]=2[F:18])[C:11]([CH3:30])([CH2:22][CH2:23][CH2:24][CH2:25][S:26]([OH:29])(=[O:28])=[O:27])[CH:10]=1)([OH:3])=[O:2].C(O[C:35](=O)[CH3:36])(=O)C>C(O)(=O)C>[F:21][C:13]1[C:14]([F:20])=[C:15]([F:19])[C:16]([F:18])=[C:17]2[C:12]=1[C:11]([CH3:30])([CH2:22][CH2:23][CH2:24][CH2:25][S:26]([OH:29])(=[O:28])=[O:27])/[C:10](=[CH:1]\[CH:4]=[CH:5]\[CH:6]=[CH:7]\[CH:8]=[N:9]\[C:35]1[CH:36]=[CH:13][CH:12]=[CH:11][CH:10]=1)/[N:9]2[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][C:1]([OH:3])=[O:2]参加物
4
反応条件
- 温度
- 120 °C
実験手順
To 1-(5-carboxypentyl)-4,5,6,7-tetrafluoro-3-methyl-3-(4-sulfobutyl)-3H-indolium (24 mg) was added N-[5-(phenylamino)-2,4-pentadienylidene monohydrochloride (13 mg), acetic anhydride (4 ml) and acetic acid (2 ml). This mixture was heated to 120° C. for 1 hour 45 minutes after which time it was cooled to room temperature. This crude reaction mixture (ca. 5 mg/ml product) was used without purification as further described.
後処理
- temperaturewas cooled to room temperature
- customThis crude reaction mixture (ca. 5 mg/ml product)
- customwas used without purification
出典と根拠
- ORDレコード
- ord-d76e5b6aa19f4ad18e9cdfe426c3c4de
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07767829B2
反応ノート
読み込み中…