Phosphate → FR-27743

HRID 703605노트

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HRID 703605 반응식
[F:1][CH2:2][CH2:3][O:4][CH2:5][C@@H:6]1[CH2:10][C@H:9]([S:11][C:12]2[C@H:18]([CH3:19])[C@H:17]3[N:14]([C:15](=[O:23])[C@@H:16]3[C@H:20]([OH:22])[CH3:21])[C:13]=2[C:24]([O:26]CC=C)=[O:25])[CH2:8][N:7]1C(OCC1C=CC([N+]([O-])=O)=CC=1)=O.C(C(CCCC)C([O-])=O)C.[Na+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.P([O-])([O-])([O-])=O.[H][H]>O1CCCC1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[OH-].[OH-].[Pd+2]>[F:1][CH2:2][CH2:3][O:4][CH2:5][C@@H:6]1[CH2:10][C@H:9]([S:11][C:12]2[C@H:18]([CH3:19])[C@H:17]3[N:14]([C:15](=[O:23])[C@@H:16]3[C@H:20]([OH:22])[CH3:21])[C:13]=2[C:24]([OH:26])=[O:25])[CH2:8][NH:7]1

참가 물질

9

반응물 5

HCID 1061PhosphateHCID 11776TriphenylphosphineHCID 23672331Sodium 2-ethylhexanoateHCID 56978753allyl (4R,5S,6S)-3-[(2S,4S)-2-(2-fluoroethyloxymethyl)-1-(4-nitrobenzyloxycarbonyl)-pyrrolidin-4-yl]thio-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 86744488FR-27743수율 53.2%

시약·촉매·용매 3

HCID 9942167Palladium hydroxide촉매HCID 178418397HCID 178418397, 화합물촉매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of allyl (4R,5S,6S)-3-[(2S,4S)-2-(2-fluoroethyloxymethyl)-1-(4-nitrobenzyloxycarbonyl)-pyrrolidin-4-yl]thio-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (4.00 g), sodium 2-ethylhexanoate (1.21 g), and triphenylphosphine (0.35 g) in tetrahydrofuran (120 ml) was added tetrakis(triphenylphosphine)palladium(0) (0.77 g) at ambient temperature in a stream of nitrogen. The mixture was stirred at the same condition for one hour. To the mixture was added 0.1M phosphate buffer (pH 6.0) (120 ml). The mixture was stirred in the presence of 20% palladium hydroxide on carbon (0.8 g) under atmospheric pressure of hydrogen at ambient temperature for 4 hours. The catalyst was filtered off and the filtrate was concentrated under reduced pressure to remove the tetrahydrofuran. An aqueous solution was washed with ethyl acetate (100 ml×3) and the organic solvent was removed by evaporation. The residual solution was subjected to a column chromatography on nonionic adsorption resin, "Diaion HP-20" (100 ml) and eluted with a mixture of acetone and water (7:93 V/V). The fractions containing the desired compound were collected and lyophilized to give (4R,5S,6S)-3-[(2S,4S)-2-(2-fluoroethyloxymethyl)pyrrolidin-4-yl]thio-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid as a solid (1.36 g). ##STR31##

후처리

  1. filtrationThe catalyst was filtered off
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customto remove the tetrahydrofuran
  4. washAn aqueous solution was washed with ethyl acetate (100 ml×3)
  5. customthe organic solvent was removed by evaporation
  6. wash" (100 ml) and eluted with a mixture of acetone and water (7:93 V/V)
  7. additionThe fractions containing the desired compound
  8. customwere collected

출처 및 근거

ORD 기록
ord-ed1c668285bb405a8538a4983d35f5ef
출처 데이터셋
uspto-grants-1991_01
특허 번호
US04983596

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