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Acetic Acid → HCID 66674145, 화합물

HRID 423407
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HRID 423407 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH2:12][CH2:11][C@@H:10]([NH2:13])[CH2:9]2)=[N:6][CH:7]=1.C(O[C:17]1(O[Si](C)(C)C)[CH2:19][CH2:18]1)C.[CH3:25][C:26](O)=O.[BH3-][C:30]#N.[Na+]>CO>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH2:12][CH2:11][C@@H:10]([N:13]([CH:17]3[CH2:18][CH2:19]3)[CH:26]3[CH2:25][CH2:30]3)[CH2:9]2)=[N:6][CH:7]=1
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6

반응물 4

HCID 176Acetic AcidHCID 2734686(1-Ethoxycyclopropoxy)trimethylsilaneHCID 5003444Sodium cyanoborohydrideHCID 53629854HCID 53629854, 화합물

생성물 1

HCID 66674145HCID 66674145, 화합물수율 56.2%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
0 °C

실험 절차

Dissolve (R)-1-(5-bromo-pyridin-2-yl)-pyrrolidin-3-ylamine (1.60 g, 6.63 mmol) in CH3OH (915 mL). Add (1-ethoxy-cyclopropoxy)-trimethyl-silane (2.7 mL, 13.49 mmol) and HOAc (1.9 mL, 33.15 mmol) and stir at RT for 3 h. Add NaBH3CN (4.2 g, 66.30 mmol) and reflux overnight. Cool the mixture to 0° C., quench with 2.0 M NaOH (15 mL), and dilute with H2O (100 mL). Extract with EtOAc (3×100 mL). Wash the combined organic layers with 1.0 M NaOH (50 mL), H2O (100 mL), and brine (50 mL). Dry the solution with Na2SO4, filter, and concentrate. Purify the crude material by chromatography, eluting with 0.5% Et3N, 5% CH3OH and 95% CHCl3 to give 1.20 g (56%) of the title compound. MS/ES m/z (79Br) 322 [M+H]+.

후처리

  1. customquench with 2.0 M NaOH (15 mL)
  2. additiondilute with H2O (100 mL)
  3. extractionExtract with EtOAc (3×100 mL)
  4. washWash the combined organic layers with 1.0 M NaOH (50 mL), H2O (100 mL), and brine (50 mL)
  5. dry with materialDry the solution with Na2SO4
  6. filtrationfilter
  7. concentrationconcentrate
  8. customPurify the crude material by chromatography
  9. washeluting with 0.5% Et3N, 5% CH3OH and 95% CHCl3

출처 및 근거

ORD 기록
ord-38f2f760ba0b4edfb0065174a5ca6a2a
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08101764B2

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