4-Methylmorpholine → HCID 20738635, 화합물

HRID 354100

반응식

HRID 354100 반응식
[Cl:1][C:2]1[N:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.[C:33]([O:37][C:38](=[O:49])[NH:39][CH2:40][C:41]1[CH:46]=[CH:45][C:44]([CH2:47][NH2:48])=[CH:43][CH:42]=1)([CH3:36])([CH3:35])[CH3:34].CN1CCOCC1>CN(C)C=O>[C:33]([O:37][C:38](=[O:49])[NH:39][CH2:40][C:41]1[CH:42]=[CH:43][C:44]([CH2:47][NH:48][C:4]([C:3]2[C:2]([Cl:1])=[N:10][CH:9]=[CH:8][CH:7]=2)=[O:6])=[CH:45][CH:46]=1)([CH3:36])([CH3:34])[CH3:35]

참가 물질

7

실험 절차

2-Chloro-nicotinic acid (2.86 g, 18.2 mmol), 1-hydroxybenzotriazole (3.0 g, 21.8 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (4.18 g, 21.8 mmol) were dissolved in N,N-dimethylformamide (50 ml) at room temperature and (4-aminomethyl-benzyl)-carbamic acid tert-butyl ester (4.29 g, 18.2 mmol) (see Preparation 1) added followed by addition of N-methyl morpholine (4 ml, 36.3 mmol). The reaction mixture was stirred under an atmosphere of nitrogen at room temperature for 18 hours, then partitioned between ethyl acetate (100 ml) and water (100 ml) and the organic layer separated. The organic layer was then washed with a saturated aqueous solution of sodium chloride (100 ml), dried over anhydrous magnesium sulphate and the solvent removed in vacuo. The residue was then triturated with diethylether (2-fold 10 ml) to give (4-{[(2-chloro-pyridine-3-carbonyl)-amino]-methyl}-benzyl)-carbamic acid tert-butyl ester (6.71 g) as a white solid.

후처리

  1. custompartitioned between ethyl acetate (100 ml) and water (100 ml)
  2. customthe organic layer separated
  3. washThe organic layer was then washed with a saturated aqueous solution of sodium chloride (100 ml)
  4. dry with materialdried over anhydrous magnesium sulphate
  5. customthe solvent removed in vacuo
  6. customThe residue was then triturated with diethylether (2-fold 10 ml)

출처 및 근거

ORD 기록
ord-64f729534280458b9a3bfb1aa91f6126
출처 데이터셋
uspto-grants-2004_06
특허 번호
US06756392B2

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