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1,1'-Carbonyldiimidazole → (S)-2-(2-amino-4-methoxy-benzoylamino)-hexanoic acid methyl ester

HRID 388475
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인쇄 미리보기

반응식

HRID 388475 반응식
[NH2:1][C:2]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.C(N1C=CN=C1)(N1C=CN=C1)=O.N12CCCN=C1CCCCC2.Cl.[CH3:37][O:38][C:39](=[O:46])[C@@H:40]([NH2:45])[CH2:41][CH2:42][CH2:43][CH3:44]>N1C=CC=CC=1.CCOC(C)=O>[CH3:37][O:38][C:39](=[O:46])[C@@H:40]([NH:45][C:4](=[O:6])[C:3]1[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:2]=1[NH2:1])[CH2:41][CH2:42][CH2:43][CH3:44]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 682631,1'-CarbonyldiimidazoleHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 3510102-Amino-4-methoxybenzoic acidHCID 14039065methyl (2S)-2-aminohexanoate hydrochloride

생성물 1

HCID 68729255(S)-2-(2-amino-4-methoxy-benzoylamino)-hexanoic acid methyl ester수율 59%

시약·촉매·용매 2

HCID 1049
Pyridine
용매
HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 2-amino-4-methoxy-benzoic acid (1.0 g, 5.98 mmol) and 1,1′-carbonyldiimidazole (980 mg, 6.04 mmol) in pyridine (5 mL) is added 1,8-diazabicyclo[5.4.0]undec-7-ene (0.9 mL, 6.02 mmol). The mixture is stirred at room temperature for 2 hours follows by the addition of (S)-2-amino-hexanoic acid methyl ester hydrochloride (1.1 g, 6.06 mmol). The reaction mixture is stirred at room temperature for 16 hours and diluted with EtOAc (100 mL), the solution is washed with H2O (50 mL×3). The organic layer is dried over sodium sulfate, and is concentrated. The resulting residue is purified by flash chromatography with 60% EtOAc in hexanes as the eluent to afford (S)-2-(2-amino-4-methoxy-benzoylamino)-hexanoic acid methyl ester (1.03 g, 59%).

후처리

  1. stirringThe reaction mixture is stirred at room temperature for 16 hours
  2. washthe solution is washed with H2O (50 mL×3)
  3. dry with materialThe organic layer is dried over sodium sulfate
  4. concentrationis concentrated
  5. customThe resulting residue is purified by flash chromatography with 60% EtOAc in hexanes as the eluent

출처 및 근거

ORD 기록
ord-8bfc118369f54071991b23aa6fcb154a
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08377949B2

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