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Acetate → Benzyloxycarbonylglycine

HRID 1416520
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인쇄 미리보기

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HRID 1416520 반응식
NCCOCCN.C([O-])(=O)C.C(=O)(O)[O-].[Na+].[CH2:17]([O:24][C:25]([NH:27][CH2:28][C:29]([O:31]C1C(F)=C(F)C(F)=C(F)C=1F)=[O:30])=[O:26])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>CN(C)C=O.O>[C:25]([NH:27][CH2:28][C:29]([OH:31])=[O:30])([O:24][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 175AcetateHCID 75982Bis(2-aminoethyl) etherHCID 516892Sodium BicarbonateHCID 10992405pentafluorophenyl N-benzyloxycarbonylglycinate

생성물 1

HCID 14349Benzyloxycarbonylglycine수율 56%

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매

실험 절차

The aminoethyl ether of Example 1 as the acetate (210 mg, 0.180 mmol) was dissolved in N,N-dimethylformamide (2 mL). To this solution 1M sodium bicarbonate (200 μL, 0.200 mmol) and pentafluorophenyl N-benzyloxycarbonylglycinate (106 mg, 0.270 mmol) were added. After 1 h, the reaction mixture was diluted with water (2×). Isolation by reverse-phase (C18) flash column chromatography eluting with 50-80% acetonitrile/water gave, after lyophilization of the product-containing fractions, the N-CBZ glycine conjugate of the above formula was obtained (130 mg):

후처리

  1. washIsolation by reverse-phase (C18) flash column chromatography eluting with 50-80% acetonitrile/water
  2. customgave

출처 및 근거

ORD 기록
ord-8d10e82f5d2c4173a3f4d967f7fefa07
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05914313

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