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Nicotinic Acid → 1-(Pyridine-3-carbonyl)-pyrrolidine-2-carboxylic acid methyl ester

HRID 82488
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HRID 82488 반응식
[CH:1]1[CH:6]=[N:5][CH:4]=[C:3]([C:7]([OH:9])=O)[CH:2]=1.[CH3:10][O:11][C:12](=[O:18])[C@@H:13]1[CH2:17][CH2:16][CH2:15][NH:14]1.CN1CCOCC1.CCN=C=NCCCN(C)C.Cl>C(Cl)Cl.CN(C1C=CN=CC=1)C>[CH3:10][O:11][C:12]([CH:13]1[CH2:17][CH2:16][CH2:15][N:14]1[C:7]([C:3]1[CH:4]=[N:5][CH:6]=[CH:1][CH:2]=1)=[O:9])=[O:18]
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참가 물질

7

반응물 4

HCID 938Nicotinic AcidHCID 79724-MethylmorpholineHCID 853477Methyl L-prolinateHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride

생성물 1

HCID 434099981-(Pyridine-3-carbonyl)-pyrrolidine-2-carboxylic acid methyl ester수율 172.9%

시약·촉매·용매 2

HCID 14284
4-(Dimethylamino)pyridine
촉매
HCID 6344Dichloromethane용매2회

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온도
25 °C

실험 절차

To a solution of niacin (0.4 g 3.50 mmol) in DCM (10 mL) were added L-proline methyl ester (0.5 g, 3.21 mmol), N-methyl morpholine (1.1 mL, 0.10.5 mmol), EDC.HCl (1.2 g, 6.4 mmol) and catalytic amount of DMAP at ice temperature (0° C.). The mixture was allowed to stir at room temperature (25° C.) over a period of 2 h. The resulting mixture diluted with DCM (100 mL) washed with water (2×100 mL) and dried over sodium sulphate. Solvent was evaporated under reduced pressure to obtain product as yellow gummy oil (1.3 g).

후처리

  1. washwashed with water (2×100 mL)
  2. dry with materialdried over sodium sulphate
  3. customSolvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-3733038fe77a4ef3b693f11951fb0d39
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846721B2

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