2,2-Dimethoxypropane → (3aR,4R,9bR)-benzyl 4-(methoxymethyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline-1-carboxylate

HRID 592103

반응식

HRID 592103 반응식
[CH3:1][O:2][CH2:3][C:4](=[C:12]1[CH2:16][CH2:15][N:14]([C:17]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[O:18])[C:13]1=O)[NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.N1C(=O)NC(=O)NC1=O.COC(OC)(C)C>CC(C)=O>[CH3:1][O:2][CH2:3][C@H:4]1[C@H:12]2[CH2:16][CH2:15][N:14]([C:17]([O:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[O:18])[C@H:13]2[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[NH:5]1

참가 물질

5

반응물 3

HCID 64952,2-DimethoxypropaneHCID 7956Cyanuric acidHCID 131734548Benzyl 3-(2-methoxy-1-(phenylamino)ethylidene)-2-oxopyrrolidine-1-carboxylate

생성물 1

HCID 117841166(3aR,4R,9bR)-benzyl 4-(methoxymethyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline-1-carboxylate

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

Into a 20 mL Schlenk flask were charged [Rh(cod)2]OTf (6.4 mg) [mw. 468.34, 0.0136 mmol, s/c 50] and (2S,4S)-3,5-xylyl-skewphos (9.0 mg) [mw. 552.71, 0.0163 mmol], and the system was substituted with argon. Deaeration-treated dehydrated acetone (5 mL) was added by argon pressure supply. Under an argon atmosphere, the mixture was stirred at room temperature for 1 hr. Separately, into a 120 mL stainless autoclave were charged benzyl 3-(2-methoxy-1-(phenylamino)ethylidene)-2-oxopyrrolidine-1-carboxylate (250.0 mg) [mw. 366.41, 0.682 mmol] and cyanuric acid (88.0 mg) [mw. 129.08, 0.682 mmol], and the system was substituted with argon. The catalyst in the Schlenk flask was added into the autoclave by argon pressure supply. A mixture of 2,2-dimethoxypropane (244 μL) [mw. 104.15, 2.05 mmol] and deaeration-treated dehydrated acetone (3 mL) added by argon pressure supply in the Schlenk flask was added into the autoclave by argon pressure supply. Furthermore, the inside of the Schlenk flask was washed with dehydrated acetone (2 mL), and the washing was added into the autoclave by argon pressure supply. Hydrogen was filled therein to 6 MPa, and the mixture was stirred at a reaction temperature of 60° C. for 16 hr. The reaction mixture was allowed to cool to room temperature and depressurized. The reaction mixture was subjected to high performance liquid chromatography and area percentage and optical purity of the resultant product, (3aR,4R,9bR)-benzyl 4-(methoxymethyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline-1-carboxylate, were determined to find production at a ratio of 95%. The optical purity was 22% ee.

후처리

  1. additionwas added by argon pressure supply
  2. additionThe catalyst in the Schlenk flask was added into the autoclave by argon pressure supply
  3. additionadded by argon pressure supply in the Schlenk flask
  4. additionwas added into the autoclave by argon pressure supply
  5. washFurthermore, the inside of the Schlenk flask was washed with dehydrated acetone (2 mL)
  6. additionthe washing was added into the autoclave by argon pressure supply
  7. additionHydrogen was filled
  8. stirringto 6 MPa, and the mixture was stirred at a reaction temperature of 60° C. for 16 hr
  9. temperatureto cool to room temperature

출처 및 근거

ORD 기록
ord-bd550823b68040c4a071ec9dd3cddf56
출처 데이터셋
uspto-grants-2016_01
특허 번호
US09238667B2

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