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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 503192, 화합물

HRID 2393520
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인쇄 미리보기

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HRID 2393520 반응식
[C:1]([NH:5][C:6]([C@@H:8]1[CH2:13][C@H:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:11][CH2:10][N:9]1[CH2:20][C@@H:21]([OH:41])[C@@H:22]([NH:30]C(OCC1C=CC=CC=1)=O)[CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[Li].[N:43]1[CH:48]=[CH:47][CH:46]=[CH:45][C:44]=1[CH2:49][O:50][C:51]([NH:53][C@H:54]([C:59]([OH:61])=O)[C@H:55]([CH2:57][CH3:58])[CH3:56])=[O:52].ON1C2C=CC=CC=2N=N1.C(N=C=NCCCN(C)C)C>CN(C=O)C.CCOCC.[Pd].CO>[C:1]([NH:5][C:6]([C@@H:8]1[CH2:13][C@H:12]([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:11][CH2:10][N:9]1[CH2:20][C@@H:21]([OH:41])[C@@H:22]([NH2:30])[CH2:23][C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1)=[O:7])([CH3:4])([CH3:2])[CH3:3].[C:1]([NH:5][C:6]([C@@H:8]1[CH2:13][C@H:12]([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:11][CH2:10][N:9]1[CH2:20][C@@H:21]([OH:41])[C@@H:22]([NH:30][C:59](=[O:61])[C@H:54]([C@H:55]([CH2:57][CH3:58])[CH3:56])[NH:53][C:51]([O:50][CH2:49][C:44]1[CH:45]=[CH:46][CH:47]=[CH:48][N:43]=1)=[O:52])[CH2:23][C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

11

반응물 5

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 503167HCID 503167, 화합물HCID 3028194LithiumHCID 54304856HCID 54304856, 화합물

생성물 2

HCID 503192HCID 503192, 화합물수율 161.8%
HCID 22870891
HCID 22870891, 화합물

시약·촉매·용매 4

HCID 23938Palladium촉매HCID 887Methanol용매HCID 3283Diethyl Ether용매HCID 6228Dimethylformamide용매

실험 절차

N-tert-butyl-1-{3(S)-amino-2(R)-hydroxy-4-phenylbutyl}-4(R)-phenylpiperidine-2(S)-carboxamide {prepared by hydrogenolysis (5% Pd/C, 1 atmosphere, MeOH, 2h) from 0.605 mg (0.108 mmol) of N-tert-butyl-1-{3(S)-(benzyloxycarbonylamino)-2(R)-hydroxy-4-phenylbutyl}-4(R)-phenylpiperidine-2(S)-carboxamide (see entry 1 of Table I)} was dissolved in DMF (1.6 mL). The lithium salt of N-{(2-pyridinylmethoxy)carbonyl}isoleucine (586 mg, 0.228 mmol), 1-hydroxybenzotriazole (32 mg, 0.237 mmol) and N-ethyl-N'-{3-(dimethylamino)propyl}carbodiimide (45.4 mg, 0.237 mmol) were added to the solution. The mixture was stirred at room temperature for 18 h. Thereafter, the reaction mixture was diluted with Et2O, washed with H2O , a saturated aqueous solution of NaHCO3 (2×) and brine, dried (MgSO4) and evaporated to dryness. The resulting yellow oil was purified by flash chromatography (SiO2, eluent: CHCl3, MeOH, 97.5:2.5 and then 95:5) to give the title compound as a white solid (58.7 mg). FAB mass spectrum, m/z: 672 (M+H)+.

후처리

  1. washwashed with H2O
  2. dry with materiala saturated aqueous solution of NaHCO3 (2×) and brine, dried (MgSO4)
  3. customevaporated to dryness
  4. customThe resulting yellow oil was purified by flash chromatography (SiO2, eluent

출처 및 근거

ORD 기록
ord-72407488692b4dcf8e281b4ca29f15c9
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05807870

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