Tetrahydrofuran → (S)-3-{[(benzyloxy)carbonyl][3-(trifluoromethyl)benzyl]amino}-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrimidine-6-carboxylic Acid

HRID 10986

反応式

HRID 10986 の反応式
[CH2:1]([O:8][C:9](=[O:41])[NH:10][C:11]1[C:16](=[O:17])[N:15]2[CH:18]([C:21](=[O:40])NCC3C=CC(C(NC(OC(C)(C)C)=O)=N)=CC=3)[CH2:19][CH2:20][C:14]2=[N:13][CH:12]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:42][C:43]([F:53])([F:52])[C:44]1[CH:45]=[C:46]([CH:49]=[CH:50][CH:51]=1)[CH2:47]Br.[H-].[Na+].C1C[O:59]CC1>CCCC[N+](CCCC)(CCCC)CCCC.[I-]>[CH2:1]([O:8][C:9]([N:10]([CH2:47][C:46]1[CH:49]=[CH:50][CH:51]=[C:44]([C:43]([F:53])([F:52])[F:42])[CH:45]=1)[C:11]1[C:16](=[O:17])[N:15]2[C@H:18]([C:21]([OH:59])=[O:40])[CH2:19][CH2:20][C:14]2=[N:13][CH:12]=1)=[O:41])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

6

反応物 4

HCID 8028TetrahydrofuranHCID 24758Sodium hydrideHCID 1230611-(Bromomethyl)-3-(trifluoromethyl)benzeneHCID 145857201benzyl N-[6-[[4-[N-[(2-methylpropan-2-yl)oxycarbonyl]carbamimidoyl]phenyl]methylcarbamoyl]-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidin-3-yl]carbamate

生成物 1

HCID 57444827(S)-3-{[(benzyloxy)carbonyl][3-(trifluoromethyl)benzyl]amino}-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrimidine-6-carboxylic Acid収率 93%

試薬・触媒・溶媒 1

HCID 67553Tetrabutylammonium Iodide触媒

実験手順

To a mixture of acid 1i (4.50 g, 13.7 mmol) in 70 mL THF at 0° C., was added 3-(trifluoromethyl)benzyl bromide (8.35 mL, 54.7 mmol), NaH (60% dispersion in oil, 1.64 g, 41.4 mmol), and TBAI (100 mg, catalytic). The reaction was stirred at rt for 15 h, then quenched with the addition of 50 mL H2O. The volatile solvents were removed by rotary evaporation and the aqueous solution obtained was partitioned with Et2O. The organic phase was extracted with 20% sat. NaHCO3 (3×). The combined aqueous extract was acidified with 1N HCl and extracted with EtOAc (5×). The combined organic extract was washed (brine), dried (Na2SO4), and concentrated to afford 6.18 g (93%) of the 3-(trifluoromethyl)benzyl amine (25a), which was used in the following step without additional purification. MS (ESI) 488.3 (M+H+), 510.3 (M+Na+); 486.3 (M−H+).

後処理

  1. customquenched with the addition of 50 mL H2O
  2. customThe volatile solvents were removed by rotary evaporation
  3. customthe aqueous solution obtained
  4. customwas partitioned with Et2O
  5. extractionThe organic phase was extracted with 20% sat. NaHCO3 (3×)
  6. extractionThe combined aqueous extract
  7. extractionextracted with EtOAc (5×)
  8. extractionThe combined organic extract
  9. washwas washed (brine)
  10. dry with materialdried (Na2SO4)
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-d0d4c49598e642f9a8b23b814d8fa918
出典データセット
uspto-grants-2006_08
特許番号
US07094783B2

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