Ethyl Acetate → Methyl N-(ethoxycarbonyl)-O-(3'-{[(propylamino)carbonyl]amino}-1,1'-biphenyl-3-yl)-L-serinate

HRID 1265222노트

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HRID 1265222 반응식
Cl.[CH2:2]([NH:5][C:6]([NH:8][C:9]1[CH:10]=[C:11]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([O:21][CH2:22][C@@H:23]([C:25]([O:27][CH3:28])=[O:26])[NH2:24])[CH:16]=2)[CH:12]=[CH:13][CH:14]=1)=[O:7])[CH2:3][CH3:4].C(N(CC)C(C)C)(C)C.[NH4+].[Cl-].[C:40]([O:43][CH2:44][CH3:45])(=[O:42])C>C1COCC1>[CH2:44]([O:43][C:40]([NH:24][C@H:23]([C:25]([O:27][CH3:28])=[O:26])[CH2:22][O:21][C:17]1[CH:16]=[C:15]([C:11]2[CH:12]=[CH:13][CH:14]=[C:9]([NH:8][C:6]([NH:5][CH2:2][CH2:3][CH3:4])=[O:7])[CH:10]=2)[CH:20]=[CH:19][CH:18]=1)=[O:42])[CH3:45]

참가 물질

6

반응물 4

HCID 8857Ethyl AcetateHCID 25517Ammonium ChlorideHCID 81531DiisopropylethylamineHCID 69940921Methyl O-(3'-{[(propylamino)carbonyl]amino}-1,1'-biphenyl-3-yl)-L-serinate Hydrochloride

생성물 1

HCID 59050114Methyl N-(ethoxycarbonyl)-O-(3'-{[(propylamino)carbonyl]amino}-1,1'-biphenyl-3-yl)-L-serinate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

The compound of Example 6 (256.0 mg, 0.63 mmol, 1 equiv) was suspended in THF (3 mL) and cooled to 0° C. Ethyl chloroformiate (88.5 mg, 0.82 mmol, 1.3 equiv) was added dropwise followed by N,N diisopropylethylamine (234.3 mg, 1.88 mmol, 3 equiv). The reaction mixture was allowed to warm to room temperature and stirred for one hour. It was worked up by addition of sat. aqueous NH4Cl soln. and ethyl acetate. The phases were separated and the organic layer was dried over NaSO4. After filtration and evaporation of the solvents the crude product was purified by chromatography (SiO2 CH/EtOAc 90:10). Yield 210.0 mg, 75.4% of a white solid. 1H NMR (CDCl3, 300 MHz) δ 7.50 (s, 1H); 7.39-7.25 (m, 3H); 7.21 (d, 1H), 7.12 (d, 1H); 7.05 (s, 1H); 6.90 (brs, 1H); 6.81 (d, 1H); 5.80 (d, 1H); 5.10 (m, 1H); 4.75-4.65 (m, 1H); 4.42 (dd, 1H); 4.25 (dd, 1H); 4.20-4.10 (m, 2H); 3.79 (s, 3H); 3.20 (dd, 2H); 1.52 (sext, 2H); 1.22 (t, 3H); 0.95 (t, 3H). MS (DCI/NH3) 461 (M+NH4), 444 (M+H).

후처리

  1. additionEthyl chloroformiate (88.5 mg, 0.82 mmol, 1.3 equiv) was added dropwise
  2. temperatureto warm to room temperature
  3. customThe phases were separated
  4. dry with materialthe organic layer was dried over NaSO4
  5. filtrationAfter filtration and evaporation of the solvents the crude product
  6. customwas purified by chromatography (SiO2 CH/EtOAc 90:10)

출처 및 근거

ORD 기록
ord-facb01c9fad74206b3c2418509bb6ea4
출처 데이터셋
uspto-grants-2003_04
특허 번호
US06545029B2

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