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Sodium Hydroxide → HCID 68834969, 화합물

HRID 747762
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HRID 747762 반응식
[C:1]1([S:7]([NH:10][C@@H:11]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([O:23][CH:24]3[CH2:29][CH2:28][N:27]([C:30]([O:32][CH2:33][C:34]4[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=4)=[O:31])[CH2:26][CH2:25]3)=[CH:19][CH:18]=2)[C:12]([O:14]C)=O)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+].Cl.Cl.[NH2:44][C:45]1[CH:46]=[C:47]([CH:51]=[CH:52][CH:53]=1)[C:48]([NH2:50])=[NH:49].CCN=C=NCCCN(C)C>CO.O1CCCC1.N1C=CC=CC=1>[C:48]([C:47]1[CH:46]=[C:45]([NH:44][C:12](=[O:14])[C@@H:11]([NH:10][S:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)(=[O:9])=[O:8])[CH2:16][C:17]2[CH:18]=[CH:19][C:20]([O:23][CH:24]3[CH2:29][CH2:28][N:27]([C:30]([O:32][CH2:33][C:34]4[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=4)=[O:31])[CH2:26][CH2:25]3)=[CH:21][CH:22]=2)[CH:53]=[CH:52][CH:51]=1)(=[NH:49])[NH2:50]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

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HCID 14798Sodium HydroxideHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 3084651m-Aminobenzamidine dihydrochlorideHCID 86760713HCID 86760713, 화합물

생성물 1

HCID 68834969HCID 68834969, 화합물

시약·촉매·용매 3

HCID 887Methanol
용매
HCID 1049Pyridine용매
HCID 8028Tetrahydrofuran용매

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온도
50 °C

실험 절차

1.75 g (3.26 mmol) of methyl (2S)-2-(benzenesulfonylamino)-3-[4-[1-(benzyloxycarbonyl)-4-piperidyloxy]phenyl]propionate was dissolved in a mixed solvent of 10 ml of methanol and 10 ml of tetrahydrofuran. 6.52 ml (6.52 mmol) of 1 N aqueous sodium hydroxide solution was added to the solution, and they were stirred at 50° C. overnight. The reaction mixture was washed with ether and then made acidic with concentrated hydrochloric acid. After the isolation process with dichloromethane as the extractant in the same manner as that of step 1 in Example 1, an oily residue was obtained, which was dissolved in 60 ml of pyridine. 747 mg (3.61 mmol) of 3-aminobenzamidine dihydrochloride and 750 mg (3.92 mmol) of WSC were added to the solution, and they were stirred at room temperature overnight. The solvent was distilled off, and the residue was purified by the silica gel column chromatography to obtain the title compound.

후처리

  1. washThe reaction mixture was washed with ether
  2. customAfter the isolation process with dichloromethane as the extractant in the same manner as that of step 1 in Example 1, an oily residue was obtained
  3. stirringwere stirred at room temperature overnight
  4. distillationThe solvent was distilled off
  5. customthe residue was purified by the silica gel column chromatography

출처 및 근거

ORD 기록
ord-6bb77e3980b54f5da2b29454cb94931d
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07396844B1

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