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HCID 70558534, 화합물 → HCID 70556450, 화합물

HRID 707681
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HRID 707681 반응식
[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C@:9]12[CH2:16][O:15][C@H:14]([CH2:17][O:18][C:19]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C@H:13]1[CH2:12][O:11][NH:10]2>C(O)(=O)C.[Zn]>[NH2:10][C@@:9]1([C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([F:8])[C:2]=2[F:1])[CH2:16][O:15][C@H:14]([CH2:17][O:18][C:19]([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[C@H:13]1[CH2:12][OH:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 70558534HCID 70558534, 화합물

생성물 1

HCID 70556450HCID 70556450, 화합물

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

Zinc powder (20.0 g) was added to a solution containing (3aR,4S,6aS)-6a-(2,3-difluorophenyl)-4-((trityloxy)methyl)hexahydrofuro[3,4-c]isoxazole, obtained in Preparation Example 1-(2), (15.51 g) in acetic acid (120 mL) at 0° C. The reaction solution was allowed to warm to RT and stirred for 18 h. The insoluble matter was separated by filtration through Celite®, washing with acetic acid (100 mL) and AcOEt (300 mL), and the filtrate was concentrated. Saturated aqueous NaHCO3 solution was added carefully to neutralize the residue, and the mixture was extracted with EtOAc (3×200 mL). The combined organic layers were dried over MgSO4 and evaporated to obtain the title compound (15.42 g). 1H-NMR (400 MHz, CDCl3) δ (ppm): 2.60-2.68 (m, 1H), 2.85 (br s, 3H), 3.29 (d, J=4.8 Hz, 2H), 3.66 (dd, J=12.1, 4.8 Hz, 1H), 3.89-3.99 (m, 2H), 4.31 (d, J=9.1 Hz, 1H), 4.34-4.40 (m, 1H), 7.04-7.19 (m, 2H), 7.20-7.33 (m, 10H), 7.39-7.50 (m, 6H)

후처리

  1. customat 0° C
  2. customThe insoluble matter was separated by filtration through Celite®
  3. washwashing with acetic acid (100 mL) and AcOEt (300 mL)
  4. concentrationthe filtrate was concentrated
  5. additionSaturated aqueous NaHCO3 solution was added carefully
  6. extractionthe mixture was extracted with EtOAc (3×200 mL)
  7. dry with materialThe combined organic layers were dried over MgSO4
  8. customevaporated

출처 및 근거

ORD 기록
ord-21d912a09d2a4496ba3885fe59e240a7
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09175013B2

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