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tert-Butyl 4-oxopiperidine-1-carboxylate → 3-[2-(1-t-Butoxycarbonyl-4-piperidinylamino)ethyl]-2-aminopyridine

HRID 1453958
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HRID 1453958 반응식
[NH2:1][CH2:2][CH2:3][C:4]1[C:5]([NH2:10])=[N:6][CH:7]=[CH:8][CH:9]=1.[C:11]([O:15][C:16]([N:18]1[CH2:23][CH2:22][C:21](=O)[CH2:20][CH2:19]1)=[O:17])([CH3:14])([CH3:13])[CH3:12].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClC(Cl)C.C(O)(=O)C>[C:11]([O:15][C:16]([N:18]1[CH2:23][CH2:22][CH:21]([NH:1][CH2:2][CH2:3][C:4]2[C:5]([NH2:10])=[N:6][CH:7]=[CH:8][CH:9]=2)[CH2:20][CH2:19]1)=[O:17])([CH3:14])([CH3:12])[CH3:13]
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참가 물질

6

반응물 3

HCID 735900tert-Butyl 4-oxopiperidine-1-carboxylateHCID 5049666Sodium triacetoxyborohydrideHCID 541059293-(2-Aminoethyl)pyridin-2-amine

생성물 1

HCID 685357713-[2-(1-t-Butoxycarbonyl-4-piperidinylamino)ethyl]-2-aminopyridine수율 42.2%

시약·촉매·용매 2

HCID 176Acetic Acid촉매
HCID 6365
1,1-Dichloroethane
용매

실험 절차

A solution of 3-(2-aminoethyl)-2-aminopyridine (0.122 g, 0.88 mmol) and 1-t-butoxycarbonyl 4-piperidone (0.177 g, 0.88 mmol) in dichloroethane (3 mL) containing 2 drops of acetic acid was treated with sodium triacetoxyborohydride (0.28 g, 1.33 mmol) at 20-75° C. until starting material was no longer consumed. The reaction was worked up with saturated sodium bicarbonate and methylene chloride, and dried over sodium sulfate. The crude product was purified by chromatography (silica gel, 0-10% {0.1% ammonium hydroxide in methanol) in methylene chloride, gradient elution) to produce the title compound (0.119 g) as a yellow oil. MS 321 (M+1).

후처리

  1. customwas no longer consumed
  2. dry with materialdried over sodium sulfate
  3. customThe crude product was purified by chromatography (silica gel, 0-10% {0.1% ammonium hydroxide in methanol) in methylene chloride
  4. washgradient elution)

출처 및 근거

ORD 기록
ord-e64ae6b86b49456fb572f5d2fcbe7ae8
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07476665B2

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