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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → [3,3-dimethyl-1(S)-(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)butyl]carbamic acid benzyl ester

HRID 907616
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HRID 907616 반응식
[CH3:1][C:2]1([CH2:6][O:7][C:8](=[O:26])[C@@H:9]([NH:15][C:16]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[O:17])[CH2:10][C:11]([CH3:14])([CH3:13])[CH3:12])[CH2:5][O:4][CH2:3]1.C(N(CC)CC)C>C(Cl)Cl.B(F)(F)F.CCOCC>[CH2:19]([O:18][C:16](=[O:17])[NH:15][C@H:9]([C:8]12[O:4][CH2:5][C:2]([CH3:1])([CH2:3][O:26]1)[CH2:6][O:7]2)[CH2:10][C:11]([CH3:12])([CH3:14])[CH3:13])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8471TriethylamineHCID 673918222(S)-benzyloxycarbonylamino-4,4-dimethylpentanoic acid 3-methyloxetan-3-ylmethyl ester

생성물 1

HCID 67391458[3,3-dimethyl-1(S)-(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)butyl]carbamic acid benzyl ester수율 72.3%

시약·촉매·용매 2

HCID 8000Boron trifluoride etherate촉매HCID 6344Dichloromethane
용매

실험 절차

To a solution of 2(S)-benzyloxycarbonylamino-4,4-dimethylpentanoic acid 3-methyl-oxetan-3-ylmethyl ester (21.5 g, 59 mmol) in dry DCM (50 ml) was added BF3.Et2O (0.4 ml, 3.2 mmol). After 5 h, triethylamine (0.9 ml, 6.4 mmol) was added and stirring was continued for 30 min at room temperature. The solvent was evaporated using a rotavap and the resulting oil was redissolved in ethyl acetate and was washed with 50 ml of 3% NH4Cl solution followed by brine. The ethyl acetate layer was dried over MgSO4, the solvent was evaporated and the residue was purified with column chromatography using silica gel and 20:80 EtOAc:Hexane as eluent to give [3,3-dimethyl-1(S)-(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)butyl]carbamic acid benzyl ester (15.5 g).

후처리

  1. waitwas continued for 30 min at room temperature
  2. customThe solvent was evaporated
  3. dissolutionthe resulting oil was redissolved in ethyl acetate
  4. washwas washed with 50 ml of 3% NH4Cl solution
  5. dry with materialThe ethyl acetate layer was dried over MgSO4
  6. customthe solvent was evaporated
  7. customthe residue was purified with column chromatography

출처 및 근거

ORD 기록
ord-2f239e58a85a4ff5b338967acd59a687
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08013186B2

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