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Hydrochloric Acid → HCID 58557318, 화합물

HRID 1969863
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HRID 1969863 반응식
O1CCO[CH:2]1[CH2:6][CH2:7][C:8]1[CH:13]=[N:12][C:11]2[N:14]([S:17]([C:20]3[CH:26]=[CH:25][C:23]([CH3:24])=[CH:22][CH:21]=3)(=[O:19])=[O:18])[CH:15]=[CH:16][C:10]=2[C:9]=1[NH:27][CH:28]1[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1.Cl.[BH4-].[Na+]>CCO>[CH:28]1([N:27]2[C:9]3[C:8](=[CH:13][N:12]=[C:11]4[N:14]([S:17]([C:20]5[CH:21]=[CH:22][C:23]([CH3:24])=[CH:25][CH:26]=5)(=[O:19])=[O:18])[CH:15]=[CH:16][C:10]4=3)[CH2:7][CH2:6][CH2:2]2)[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 4311764Sodium borohydrideHCID 58557742HCID 58557742, 화합물

생성물 1

HCID 58557318HCID 58557318, 화합물수율 75.7%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
40 °C

실험 절차

To a solution of 5-(2-(1,3-dioxolan-2-yl)ethyl)-N-cyclohexyl-1-tosyl-1H-pyrrolo[2,3-b]pyridin-4-amine (0.209 g, 0.445 mmol) in EtOH (2 mL) was added aqueous HCl (12 N, 0.186 mL, 2.23 mmol) dropwise. The mixture was heated at about 40° C. for about 2 h and then cooled to about 0° C. in an ice bath. Sodium borohydride (0.118 g, 3.12 mmol) was added portionwise and the mixture was warmed to ambient temperature. After about 2 h the solvent was removed under reduced pressure and the residue was partitioned between EtOAc and saturated aqueous NaHCO3 (10 mL each). The aqueous phase was extracted with EtOAc (2×5 mL) and the combined organics were washed with water and brine (5 mL each), dried over anhydrous Na2SO4, filtered and concd under reduced pressure. The residue was purified by silica gel chromatography eluting with 0-50% EtOAc in heptane to give 1-cyclohexyl-7-tosyl-2,3,4,7-tetrahydro-1H-pyrrolo[2,3-h]-[1,6]naphthyridine (0.138 g, 75%) as a white solid: LC/MS (Table 1, Method b) Rt=3.01 min; MS m/z: 410 (M+H)+.

후처리

  1. temperaturecooled to about 0° C. in an ice bath
  2. temperaturethe mixture was warmed to ambient temperature
  3. customAfter about 2 h the solvent was removed under reduced pressure
  4. customthe residue was partitioned between EtOAc and saturated aqueous NaHCO3 (10 mL each)
  5. extractionThe aqueous phase was extracted with EtOAc (2×5 mL)
  6. washthe combined organics were washed with water and brine (5 mL each)
  7. dry with materialdried over anhydrous Na2SO4
  8. filtrationfiltered
  9. customThe residue was purified by silica gel chromatography
  10. washeluting with 0-50% EtOAc in heptane

출처 및 근거

ORD 기록
ord-974c553a3a0042c898391b80bb4fe4a3
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08426411B2

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