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Triethylamine → HCID 22914784、化合物

HRID 1534582
ノート
印刷プレビュー

反応式

HRID 1534582 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:15](=[C:16]3[CH2:21][CH2:20][N:19](C)[CH2:18][CH2:17]3)[C:10]3=[N:11][CH:12]=[CH:13][CH:14]=[C:9]3[CH:8]=[CH:7][C:6]=2[CH:23]=1.C(N(CC)CC)C.Cl[C:32]([O:34][CH2:35][C:36]([Cl:39])([Cl:38])[Cl:37])=[O:33].ClC([O-])=O>C1(C)C=CC=CC=1.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:15](=[C:16]3[CH2:17][CH2:18][N:19]([C:32]([O:34][CH2:35][C:36]([Cl:39])([Cl:38])[Cl:37])=[O:33])[CH2:20][CH2:21]3)[C:10]3=[N:11][CH:12]=[CH:13][CH:14]=[C:9]3[CH:8]=[CH:7][C:6]=2[CH:23]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8471Triethylamine2 回HCID 870632,2,2-Trichloroethyl chloroformateHCID 21226386CarbonochloridateHCID 229147865,6-Dehydro-N-methyl Desloratadine

生成物 1

HCID 22914784HCID 22914784、化合物収率 56.4%

試薬・触媒・溶媒 2

HCID 962Water
溶媒
HCID 1140Toluene溶媒

反応条件

温度
90 °C

実験手順

To a mixture of 755 mg (2.34 mmole) of 8-chloro-11-(1-methyl-4-piperidylidene)-11H-benzo[5,6]cyclohepta[1,2-b]pyridine and 1.5 mL of triethylamine in 25 mL of dry toluene at room temperature and under a nitrogen atmosphere was added 650 μL (4.72 mmole) of 2,2,2-trichloroethyl chloroformate. The mixture was then heated to 90° C. Additional amounts of the chloroformate (500 μL and 300 μL) and triethylamine (1.0 mL each time) were added to the mixture after 2 hr. and 3 hr. 40 min., respectively. After a total reaction time of 5 hr. the mixture was poured into water and extracted three times with CH2Cl2. The combined organic portions were dried over MgSO4, filtered and concentrated in vacuo. The residue was purified via flash chromatography [11/2% MeOH in CH2Cl2 ] to afford 639 mg (56%) of the title compound as a glass.

後処理

  1. custom3 hr
  2. custom40 min.
  3. customAfter a total reaction time of 5 hr
  4. extractionextracted three times with CH2Cl2
  5. dry with materialThe combined organic portions were dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified via flash chromatography [11/2% MeOH in CH2Cl2 ]

出典と根拠

ORDレコード
ord-b4c1e48b16954883bc8f6116d956a546
出典データセット
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05089496

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート