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Water → o-Carbamoyl-alpha-(1-piperazinyl)acetanilide dihydrochloride

HRID 1381189
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HRID 1381189 반응식
[ClH:1].Cl.[C:3]([C:6]1[CH:28]=[CH:27][CH:26]=[CH:25][C:7]=1[NH:8][C:9](=[O:24])[CH2:10][N:11]1[CH2:16][CH2:15][N:14](CC2C=CC=CC=2)[CH2:13][CH2:12]1)(=[O:5])[NH2:4].O>[C].[Pd].CO>[ClH:1].[ClH:1].[C:3]([C:6]1[CH:28]=[CH:27][CH:26]=[CH:25][C:7]=1[NH:8][C:9](=[O:24])[CH2:10][N:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1)(=[O:5])[NH2:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 962WaterHCID 23323546o-Carbamoyl-alpha-(4-benzyl-1-piperazinyl)acetanilide dihydrochloride

생성물 1

HCID 23323544o-Carbamoyl-alpha-(1-piperazinyl)acetanilide dihydrochloride

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 887Methanol용매

실험 절차

50 Grams of o-carbamoyl-α-(4-benzyl-1-piperazinyl)acetanilide dihydrochloride, 4 g of 10%-palladium carbon, 70 ml of water and 300 ml of methanol were mixed together and the mixture was subjected to catalytic reduction at a room temperature. Then the catalyst was removed from the mother liquor, and the mother liquor was concentrated to dryness. The residue obtained was crystallized by adding acetone, and recrystallized from water-acetone to obtain 35.2 g of o-carbamoyl-α-(1-piperazinyl)acetanilide dihydrochloride. Colorless cotton fiber-like crystals. Melting point: 239.5°-242° C. (decomposed).

후처리

  1. customwas subjected to catalytic reduction at a room temperature
  2. customThen the catalyst was removed from the mother liquor
  3. concentrationthe mother liquor was concentrated to dryness
  4. customThe residue obtained
  5. customwas crystallized
  6. additionby adding acetone
  7. customrecrystallized from water-acetone

출처 및 근거

ORD 기록
ord-061e8e3a43bd40c9a67e4ffdd8c6e4d1
출처 데이터셋
uspto-grants-1986_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04585774

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