Triethylamine → HCID 67951153, 화합물

HRID 923657노트

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HRID 923657 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]2[S:9][NH:10][C:11](=[O:12])[C:3]=12.I[CH2:14][C:15]([N:17]1[CH2:22][CH2:21][N:20]([C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:19][CH2:18]1)=[O:16].CCN(CC)CC.C([O-])([O-])=O.[Cs+].[Cs+]>C(Cl)Cl>[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]2[S:9][N:10]=[C:11]([O:12][CH2:14][C:15]([N:17]3[CH2:22][CH2:21][N:20]([C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:19][CH2:18]3)=[O:16])[C:3]=12

참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 10796Cesium carbonateHCID 173760Isothiazolo(5,4-b)pyridin-3(2H)-one, 4,6-dimethyl-HCID 67811489HCID 67811489, 화합물

생성물 1

HCID 67951153HCID 67951153, 화합물수율 11%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Pyridinothiazolone 4 (300 mg, 1.66 mmol) was treated with ethyl 4-(2-iodoacetyl)piperazine-1-carboxylate (541 mg, 1.66 mmol), Et3N (840 mg, 8.30 mmol) and Cs2CO3 (500 mg, 1.54 mmol) in anhydrous CH2Cl2 (25 mL) at room temperature for 24 h, and then washed with H2O. The organic layer was dried over MgSO4, filtered, concentrated, and purified by flash chromatography on a silica gel column (EtOAc/hexane (1:1)) to give the title compound (68 mg, 11% yield) in addition to the main N-alkylation product 21 (YMU1, 60%). The purity of product 28 was 99.5% as shown by HPLC on an HC-C18 column (Agilent, 4.6×250 mm, 5 μM), tR=4.9 min (gradients of 40-90% aqueous CH3CN in 15 min).

후처리

  1. washwashed with H2O
  2. dry with materialThe organic layer was dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. custompurified by flash chromatography on a silica gel column (EtOAc/hexane (1:1))

출처 및 근거

ORD 기록
ord-a7809249720042b0825a19f44a8b606d
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09278982B2

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