Methanimidamide, N,N-diphenyl- → HCID 73681571、化合物
反応式
[Br-:1].[OH:2][CH2:3][CH2:4][N+:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:8]([CH3:15])=[CH:7][CH:6]=1.C1(N(C2C=CC=CC=2)C=N)C=CC=CC=1.[Br-].[OH:32][CH2:33][CH2:34][N+:35]1[C:44]2[C:39](=[CH:40][CH:41]=[CH:42][CH:43]=2)[C:38]([CH:45]=[CH:46]NC2C=CC=CC=2)=[CH:37][CH:36]=1>C(O)C>[Br-:1].[OH:2][CH2:3][CH2:4][N+:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:8]([CH:15]=[CH:46][CH:45]=[C:38]2[C:39]3[C:44](=[CH:43][CH:42]=[CH:41][CH:40]=3)[N:35]([CH2:34][CH2:33][OH:32])[CH:36]=[CH:37]2)=[CH:7][CH:6]=1参加物
実験手順
On an oil bath, 2.7 g of 1-(2-hydroxyethyl)-4-methylquinolinium bromide and diphenylformamidine were heated for 5 minutes to melt them. Thereto was added 150 ml of ethanol, and the resulting mixture was boiled, upon which 1-(2-hydroxyethyl)-4-(2-anilinovinyl)-quinolinium bromide was crystallized. Then, 2.5 g of 1-hydroxyethyl-4-methylquinolinium bromide and 10 ml of triethylamine were added thereto and subjected to reaction under reflux for one hour. After completion of the reaction, the reaction product was cooled and the crude crystals thus obtained were recrystallized from methanol to obtain 2 g of the objective compound (melting point 262° C.) which was dark green. Its maximum absorption wavelength as measured in methanol was 707 nm.
後処理
- customwas crystallized
- additionThen, 2.5 g of 1-hydroxyethyl-4-methylquinolinium bromide and 10 ml of triethylamine were added
- customsubjected to reaction
- temperatureunder reflux for one hour
- customAfter completion of the reaction
- temperaturethe reaction product was cooled
- customthe crude crystals thus obtained
- customwere recrystallized from methanol
出典と根拠
- ORDレコード
- ord-abc1f3a6e629414085d9452d80fcc2e9
- 出典データセット
- uspto-grants-1983_05
- 特許番号
- US04386146
反応ノート
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