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N-BOC-ethylenediamine → t-Butyl [2-(4-nitropyridine-2-carboxamido)ethyl]carbamate

HRID 34934
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HRID 34934 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][N:7]=[C:6]([C:10]([OH:12])=O)[CH:5]=1)([O-:3])=[O:2].[NH2:13][CH2:14][CH2:15][NH:16][C:17](=[O:23])[O:18][C:19]([CH3:22])([CH3:21])[CH3:20]>O1CCCC1.C(N1C=CN=C1)(N1C=CN=C1)=O>[N+:1]([C:4]1[CH:9]=[CH:8][N:7]=[C:6]([C:10]([NH:13][CH2:14][CH2:15][NH:16][C:17](=[O:23])[O:18][C:19]([CH3:21])([CH3:20])[CH3:22])=[O:12])[CH:5]=1)([O-:3])=[O:2]
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참가 물질

5

반응물 2

HCID 187201N-BOC-ethylenediamineHCID 27628254-Nitropicolinic Acid

생성물 1

HCID 13800214t-Butyl [2-(4-nitropyridine-2-carboxamido)ethyl]carbamate

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 682631,1'-Carbonyldiimidazole용매

실험 절차

6.0 g of 4-nitro-2-pyridinecarboxylic acid were stirred at 60° bath temperature for 4 hours in 300 ml of absolute tetrahydrofuran and 5.9 g of 1,1'-carbonyldiimidazole. Thereafter, 6.0 g of t-butyl (2-aminoethyl)carbamate were added thereto and the mixture was heated to reflux for 4 hours. The reaction mixture was concentrated under reduced pressure and thereafter partitioned between ethyl acetate and water. The combined organic phases were dried over magnesium sulfate and concentrated. The residue was crystallized from ethyl acetate, whereby there was obtained t-butyl [2-(4-nitropyridine-2-carboxamido)ethyl]carbamate as white crystals, m.p. 130°-131°.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 4 hours
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. custompartitioned between ethyl acetate and water
  5. dry with materialThe combined organic phases were dried over magnesium sulfate
  6. concentrationconcentrated
  7. customThe residue was crystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-fdc7726315f94918a8ab532547c21886
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04764522

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