Hydrogen Bromide → HCID 14097029, 화합물

HRID 4319노트

반응식

HRID 4319 반응식
C[O:2][C:3]1[CH:33]=[CH:32][C:6]([CH2:7][N:8]2[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][CH2:16][N:17]3[CH2:22][CH2:21][N:20]([CH2:23][C:24]4[CH:29]=[CH:28][C:27]([O:30]C)=[CH:26][CH:25]=4)[CH2:19][CH2:18]3)[CH2:10][CH2:9]2)=[CH:5][CH:4]=1.Br>O>[OH:30][C:27]1[CH:26]=[CH:25][C:24]([CH2:23][N:20]2[CH2:21][CH2:22][N:17]([CH2:16][CH2:15][CH2:14][N:11]3[CH2:10][CH2:9][N:8]([CH2:7][C:6]4[CH:5]=[CH:4][C:3]([OH:2])=[CH:33][CH:32]=4)[CH2:13][CH2:12]3)[CH2:18][CH2:19]2)=[CH:29][CH:28]=1

참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 140970281,3-Bis[4-(4-methoxybenzyl)-1-piperazinyl]propane

생성물 1

HCID 14097029HCID 14097029, 화합물수율 31%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 4.5 g of 1,3-bis[4-(4-methoxybenzyl)-1-piperazinyl]propane from Example 19 and 125 ml of 49% hydrobromic acid was refluxed for 2 hours and was then cooled and diluted with 125 ml of water. After filtration the aqueous solution was neutralized with 2N sodium hydroxide to adjust the pH to 8. The resulting mixture was extracted three times each with 150 ml of ethanol. The alcohol was then removed by rotary evaporation and the residue was chromatographed on silica with the eluant being methylene chloride containing 1% ammonium hydroxide and 10% methanol to obtain 1.3 g (31% of theory) of 1,3-bis[4-(4-hydroxybenzyl)-1-piperazinyl]propane as a white crystalline product, melting at 197°-201° C.

후처리

  1. temperaturewas refluxed for 2 hours
  2. temperaturewas then cooled
  3. filtrationAfter filtration the aqueous solution
  4. extractionThe resulting mixture was extracted three times each with 150 ml of ethanol
  5. customThe alcohol was then removed by rotary evaporation
  6. customthe residue was chromatographed on silica with the eluant

출처 및 근거

ORD 기록
ord-35f81a39a06a45d1ab9c40a8e88e5022
출처 데이터셋
uspto-grants-1988_02
특허 번호
US04725597

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