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Norcamphor → 1'-(bicyclo[2.2.1]heptan-2-yl)-N-(pentan-3-yl)spiro[indene-1,4'-piperidine]-3-carboxamide

HRID 2267117
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HRID 2267117 반응식
[CH3:1][CH2:2][CH:3]([NH:6][C:7]([C:9]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[C:11]2([CH2:16][CH2:15][NH:14][CH2:13][CH2:12]2)[CH:10]=1)=[O:8])[CH2:4][CH3:5].[C@H:23]12[CH2:29][C@H:26]([CH2:27][CH2:28]1)[CH2:25][C:24]2=O.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClC(Cl)C.CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-]>[CH:23]12[CH2:29][CH:26]([CH2:27][CH2:28]1)[CH2:25][CH:24]2[N:14]1[CH2:13][CH2:12][C:11]2([C:17]3[C:22](=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:9]([C:7]([NH:6][CH:3]([CH2:2][CH3:1])[CH2:4][CH3:5])=[O:8])=[CH:10]2)[CH2:16][CH2:15]1
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참가 물질

6

반응물 3

HCID 449588NorcamphorHCID 5049666Sodium triacetoxyborohydrideHCID 25012980N-(pentan-3-yl)spiro[indene-1,4'-piperidine]-3-carboxamide

생성물 1

HCID 250120031'-(bicyclo[2.2.1]heptan-2-yl)-N-(pentan-3-yl)spiro[indene-1,4'-piperidine]-3-carboxamide

시약·촉매·용매 2

HCID 11026Titanium isopropoxide촉매
HCID 6365
1,1-Dichloroethane
용매

실험 절차

A mixture of (F2) (0.020 g, 0.05 mmol), titanium (IV) isopropoxide (0.045 mL, 0.15 mmol) and (1R,4S)-bicyclo[2.2.1]heptan-2-one (3 eq) was stirred at room temperature for 18 h in dichloroethane (0.5 mL). Sodium triacetoxyborohydride (0.011 g, 0.050 mmol) was added and the mixture stirred at room temperature for 1 h. The solvent was evaporated and 6N NaOH (0.5 mL) and methanol (1 mL) was added and then triturated to give a white solid that was washed with methanol (1 mL) and EtOAc (1 mL). The filtrate was concentrated under reduced pressure to afford the crude product which was purified by reverse phase preparative HPLC to afford 1′-(bicyclo[2.2.1]heptan-2-yl)-N-(pentan-3-yl)spiro[indene-1,4′-piperidine]-3-carboxamide (Compound No. 14) (0.013 g). LC/MS (10-90% over 3 min with 0.9% FA) m/z 324.1 (M+1), retention time 2.2 minutes.

후처리

  1. customThe solvent was evaporated
  2. addition6N NaOH (0.5 mL) and methanol (1 mL) was added
  3. customtriturated
  4. customto give a white solid
  5. washthat was washed with methanol (1 mL) and EtOAc (1 mL)
  6. concentrationThe filtrate was concentrated under reduced pressure
  7. customto afford the crude product which
  8. customwas purified by reverse phase preparative HPLC

출처 및 근거

ORD 기록
ord-c49b317282534b7ea482afc586683ca0
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07858790B2

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