Hydrochloric Acid → (7-Chloro-quinolin-4-yl)-(3-piperidin-1-yl-propyl)-amine

HRID 234687

反応式

HRID 234687 の反応式
[N:1]1([CH2:7][CH2:8][CH2:9][NH2:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl[C:12]1[C:21]2[C:16](=[CH:17][C:18]([Cl:22])=[CH:19][CH:20]=2)[N:15]=[CH:14][CH:13]=1.Cl.C1(N)C(F)=C(F)C(F)=C(N)C=1F.Cl.Cl>C(#N)C>[Cl:22][C:18]1[CH:17]=[C:16]2[C:21]([C:12]([NH:10][CH2:9][CH2:8][CH2:7][N:1]3[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]3)=[CH:13][CH:14]=[N:15]2)=[CH:20][CH:19]=1

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 68664,7-DichloroquinolineHCID 19049Piperidine-1-propylamineHCID 149026Tetrafluoro-m-phenylenediamine dihydrochloride

生成物 1

HCID 10913722(7-Chloro-quinolin-4-yl)-(3-piperidin-1-yl-propyl)-amine

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

2.73 g from 2.83 g of 3-(piperidin-1-yl)-propylamine and 3.94 g of 4,7-dichloroquinoline (reaction duration, 16 hours at 140° C.); the base (yellowish crystals from acetonitrile, m.p.: 113°-116° C.) was converted with isopropanolic hydrochloric acid into the dihydrochloride which when recrystallized from acetonitrile/ethanol, yielded colourless crystals, m.p.: 137°-141° C.

後処理

  1. customrecrystallized from acetonitrile/ethanol
  2. customyielded colourless crystals, m.p.: 137°-141° C.

出典と根拠

ORDレコード
ord-30c5f25c52664d9c892ac049451b9f1a
出典データセット
uspto-grants-1997_01
特許番号
US05596002

関連ノート

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