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Ethyl 4-piperidinecarboxylate → Ethyl 1-{isopropyl[3-({3-[(4-{3-[4-(methoxycarbonyl)phenyl]propyl}phenyl)carbamoyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}carbamoyl)benzyl]carbamoyl}piperidine-4-carboxylate

HRID 2176017
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HRID 2176017 반응식
[CH:1]([NH:4][CH2:5][C:6]1[CH:7]=[C:8]([CH:43]=[CH:44][CH:45]=1)[C:9]([NH:11][C:12]1[S:13][C:14]2[CH2:42][CH2:41][CH2:40][CH2:39][C:15]=2[C:16]=1[C:17]([NH:19][C:20]1[CH:25]=[CH:24][C:23]([CH2:26][CH2:27][CH2:28][C:29]2[CH:38]=[CH:37][C:32]([C:33]([O:35][CH3:36])=[O:34])=[CH:31][CH:30]=2)=[CH:22][CH:21]=1)=[O:18])=[O:10])([CH3:3])[CH3:2].Cl[C:47](Cl)([O:49]C(=O)OC(Cl)(Cl)Cl)Cl.[NH:58]1[CH2:68][CH2:67][CH:61]([C:62]([O:64][CH2:65][CH3:66])=[O:63])[CH2:60][CH2:59]1.C(=O)([O-])O.[Na+]>C(N(CC)CC)C.C1COCC1>[CH:1]([N:4]([CH2:5][C:6]1[CH:45]=[CH:44][CH:43]=[C:8]([C:9](=[O:10])[NH:11][C:12]2[S:13][C:14]3[CH2:42][CH2:41][CH2:40][CH2:39][C:15]=3[C:16]=2[C:17](=[O:18])[NH:19][C:20]2[CH:25]=[CH:24][C:23]([CH2:26][CH2:27][CH2:28][C:29]3[CH:30]=[CH:31][C:32]([C:33]([O:35][CH3:36])=[O:34])=[CH:37][CH:38]=3)=[CH:22][CH:21]=2)[CH:7]=1)[C:47]([N:58]1[CH2:59][CH2:60][CH:61]([C:62]([O:64][CH2:65][CH3:66])=[O:63])[CH2:67][CH2:68]1)=[O:49])([CH3:3])[CH3:2]
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참가 물질

7

반응물 4

HCID 70770Ethyl 4-piperidinecarboxylateHCID 94429TriphosgeneHCID 516892Sodium BicarbonateHCID 90370278Methyl 4-{3-[4-({[2-({3-[(isopropylamino)methyl]benzoyl}amino)-4,5,6,7-tetrahydro-1-benzothiophen-3-yl]carbonyl}amino)phenyl]propyl}benzoate

생성물 1

HCID 90370183
Ethyl 1-{isopropyl[3-({3-[(4-{3-[4-(methoxycarbonyl)phenyl]propyl}phenyl)carbamoyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}carbamoyl)benzyl]carbamoyl}piperidine-4-carboxylate

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8471Triethylamine용매

실험 절차

To a mixture of 150 mg of methyl 4-{3-[4-({[2-({3-[(isopropylamino)methyl]benzoyl}amino)-4,5,6,7-tetrahydro-1-benzothiophen-3-yl]carbonyl}amino)phenyl]propyl}benzoate and 3.5 mL of THF was added 0.045 mL of triethylamine and 28 mg of triphosgene under ice cooling, followed by stirring for 3 hours at room temperature. Thereafter, 0.080 mL of ethyl isonipecotate was added to the reaction mixture, followed by stirring for 18 hours at room temperature. An aqueous sodium hydrogen carbonate solution was added to the reaction mixture, followed by stirring for 1 hour at room temperature, and then extraction was performed using chloroform. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by basic silica gel column chromatography (NH silica gel manufactured by FUJI SILYSIA CHEMICAL LTD. (amino type silica gel (treated with aminopropyl)), (hexane:ethyl acetate=1:1)), thereby obtaining 178 mg of ethyl 1-{isopropyl[3-({3-[(4-{3-[4-(methoxycarbonyl)phenyl]propyl}phenyl)carbamoyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}carbamoyl)benzyl]carbamoyl}piperidine-4-carboxylate.

후처리

  1. stirringby stirring for 18 hours at room temperature
  2. stirringby stirring for 1 hour at room temperature
  3. extractionextraction
  4. washThe organic layer was washed with saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was removed under reduced pressure
  7. customThe residue was purified by basic silica gel column chromatography (NH silica gel manufactured by FUJI SILYSIA CHEMICAL LTD. (amino type silica gel (treated with aminopropyl)), (hexane:ethyl acetate=1:1))

출처 및 근거

ORD 기록
ord-b50b2a18cadf4f548bcc485375c629fd
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062032B2

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