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Hydrochloric Acid → Methyl (S)-2-(Boc-amino)-4-iodobutanoate

HRID 1755489
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HRID 1755489 반응식
[NH2:1][C@@H:2]([CH2:7][CH2:8]Br)[C:3]([O:5][CH3:6])=[O:4].Cl.C(N(CC)C(C)C)(C)C.[C:20]([O:24][C:25]([O:27]C(OC(C)(C)C)=O)=O)([CH3:23])([CH3:22])[CH3:21].[I-:35].[Na+]>C1COCC1>[C:20]([O:24][C:25]([NH:1][C@@H:2]([CH2:7][CH2:8][I:35])[C:3]([O:5][CH3:6])=[O:4])=[O:27])([CH3:23])([CH3:22])[CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 5238Sodium IodideHCID 81531DiisopropylethylamineHCID 90495Di-tert-butyl dicarbonateHCID 1512645(S)-methyl 2-amino-4-bromobutanoate

생성물 1

HCID 14394150Methyl (S)-2-(Boc-amino)-4-iodobutanoate수율 60%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To an ice cold suspension of (S)-methyl 2-amino-4-bromobutanoate, 1.00 HCl (see WO2003/101948 A2, 4.42 g, 19.02 mmol) and N,N-diisopropylethylamine (9.97 mL, 57.1 mmol) in anhydrous THF (50 mL) is slowly added a solution of di-tert-butyldicarbonate (4.36 g, 19.97 mmol) in anhydrous THF (8 mL). The reaction is stirred for 18 h while warming to room temp. The solvent is removed in vacuo, and the residue is partitioned between EtOAc (450 mL) and aqueous saturated ammonium chloride (30 ml). The organic layer is washed with aqueous saturated sodium bicarbonate (1×30 mL), water (1×30 mL), brine (1×30 mL), dried over Na2SO4, filtered and evaporated to dryness. The residue is dissolved in acetone (450 mL). treated with sodium iodide (14.25 g, 95.1 mmol) and the reaction is refluxed for 18 h. The reaction is cooled to room temp, filtered thru a ground glass frit and the solvent removed in vacuo. The residue is dissolved in EtOAc (450 mL), washed with water (3×40 mL), brine (1×40 mL), dried over Na2SO4, filtered, evaporated to dryness and purified by BIOTAGE® Silica gel chromatography on a 80 g Thompson Single Step silica cartridge using 100% CH2Cl2 over 10 column volumes to give 3.9 g (60%) of the title compound as a thick oil. LC/MS (Condition A): ret. T=3.40 min, (M+Na) 366.

후처리

  1. customThe solvent is removed in vacuo
  2. customthe residue is partitioned between EtOAc (450 mL) and aqueous saturated ammonium chloride (30 ml)
  3. washThe organic layer is washed with aqueous saturated sodium bicarbonate (1×30 mL), water (1×30 mL), brine (1×30 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. customevaporated to dryness
  7. dissolutionThe residue is dissolved in acetone (450 mL)
  8. temperaturethe reaction is refluxed for 18 h
  9. temperatureThe reaction is cooled to room temp
  10. filtrationfiltered thru a ground glass frit
  11. customthe solvent removed in vacuo
  12. dissolutionThe residue is dissolved in EtOAc (450 mL)
  13. washwashed with water (3×40 mL), brine (1×40 mL)
  14. dry with materialdried over Na2SO4
  15. filtrationfiltered
  16. customevaporated to dryness
  17. custompurified by BIOTAGE® Silica gel chromatography on a 80 g Thompson Single Step silica cartridge

출처 및 근거

ORD 기록
ord-989fdc351bbd4fd887b5c4b420ca943b
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09169295B2

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