1-Phenylpiperazine → 5,6-Dihydro-3-(4-phenylpiperazin-1-yl)benzo[h]cinnoline

HRID 558179ノート

反応式

HRID 558179 の反応式
Cl[C:2]1[N:3]=[N:4][C:5]2[C:6]3[CH:15]=[CH:14][CH:13]=[CH:12][C:7]=3[CH2:8][CH2:9][C:10]=2[CH:11]=1.[C:16]1([N:22]2[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.Cl.[NH4+]>>[C:16]1([N:22]2[CH2:27][CH2:26][N:25]([C:2]3[N:3]=[N:4][C:5]4[C:6]5[CH:15]=[CH:14][CH:13]=[CH:12][C:7]=5[CH2:8][CH2:9][C:10]=4[CH:11]=3)[CH2:24][CH2:23]2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

参加物

4

反応物 3

HCID 70961-PhenylpiperazineHCID 104433233-Chloro-5,6-dihydrobenzo[h]cinnolineHCID 21905121Ammonium hydrochloride

生成物 1

HCID 116025935,6-Dihydro-3-(4-phenylpiperazin-1-yl)benzo[h]cinnoline収率 88.1%

反応条件

温度
130 °C

実験手順

A mixture of comprising about 0.01 mol of 3-chloro-5,6-dihydrobenzo[h]cinnoline, about 0.05 mol of 1-phenylpiperazine and about 0.01 mol of ammonium hydrochloride was prepared in about 15 ml of 1-BuOH. The mixture was stirred at 130° C. for 48 h, and then the solvent was removed under reduced pressure. The remaining residue was then extracted with ethyl acetate, washed with water and brine, dried over anhydrous Na2SO4. Removal of solvent followed by recrystallization from 95% ethanol yielded bright yellow crystals, yield 88.1%; HPLC: 96.0% purity; HRMS calculated 342.1839, found 342.1831; 1H NMR (CDCl3): δ 8.474 (d, J=7.5, 1H), 7.222-7.400 (m, 4H), 7.012 (d, J=10, 2H), 6.925 (t, J=6.5, 3=7.5, 1H), 6.824 (S, 1H), 3.900 (s, 4H), 3.370 (d, J=4.5, 4H), 2.932 (s, 4H).

後処理

  1. customthe solvent was removed under reduced pressure
  2. extractionThe remaining residue was then extracted with ethyl acetate
  3. washwashed with water and brine
  4. dry with materialdried over anhydrous Na2SO4
  5. customRemoval of solvent
  6. customfollowed by recrystallization from 95% ethanol yielded bright yellow crystals, yield 88.1%

出典と根拠

ORDレコード
ord-c98bbbbf772b401eb0a437cc623f47f6
出典データセット
uspto-grants-2011_11
特許番号
US08063047B2

反応ノート

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