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Hydrochloric Acid → HCID 58557318、化合物

HRID 1969863
ノート
印刷プレビュー

反応式

HRID 1969863 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 4311764Sodium borohydrideHCID 58557742HCID 58557742、化合物

生成物 1

HCID 58557318HCID 58557318、化合物収率 75.7%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
40 °C

実験手順

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)+.

後処理

  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

出典と根拠

ORDレコード
ord-974c553a3a0042c898391b80bb4fe4a3
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08426411B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート