Ammonium Chloride → HCID 59497521, 화합물

HRID 1747371

반응식

HRID 1747371 반응식
[CH2:1]([NH:8][C@@H:9]([CH3:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Li]CCCC.[C:22]([O:29][CH2:30][CH3:31])(=[O:28])/[CH:23]=[CH:24]/[CH2:25][CH2:26][CH3:27].[NH4+].[Cl-]>C1COCC1>[CH2:30]([O:29][C:22](=[O:28])[CH2:23][C@@H:24]([N:8]([CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C@H:9]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH3:16])[CH2:25][CH2:26][CH3:27])[CH3:31]

참가 물질

6

반응물 4

HCID 25517Ammonium ChlorideHCID 1268085(S)-(-)-N-Benzyl-1-phenylethylamineHCID 5364778Ethyl trans-2-hexenoateHCID 178418339Butyllithium

생성물 1

HCID 59497521HCID 59497521, 화합물수율 50.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of (S)-(−)-N-benzyl-alpha-methyl-benzylamine (50 mL, 239 mmol) in THF (150 mL) at 0 C was added BuLi (2.5 M in THF) (100 mL, 250 mmol) under nitrogen atmosphere. The solution was cooled to −78 C and ethyl trans-2-hexenoate (16.6 g, 117 mmol) was added. The solution was stirred for 1 hour and Sat. NH4Cl solution was added. The solution was warmed to room temperature and was extracted with EtOAc. The combined organic layer was dried with MgSO4 and was filtered. The filtrate was concentrated and the residue was purified by CombiFlash with 5% EtOAc in Hexane as the eluent to afford the desirable product (S)-3-[Benzyl-((S)-1-phenyl-ethyl)-amino]-hexanoic acid ethyl ester (20.8 g, 50%) as a colorless oil.

후처리

  1. additionwas added
  2. extractionwas extracted with EtOAc
  3. dry with materialThe combined organic layer was dried with MgSO4
  4. filtrationwas filtered
  5. concentrationThe filtrate was concentrated
  6. customthe residue was purified by CombiFlash with 5% EtOAc in Hexane as the eluent

출처 및 근거

ORD 기록
ord-9d0e450047d74117a4b27ba2f4a828ad
출처 데이터셋
uspto-grants-2015_10
특허 번호
US09150556B2

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