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Triethylamine → benzyl((1R,2S)-2-{[((2RS)-6-fluoro-1,2,3,4-tetrahydronaphthalen-2-yl)amino]methyl}cyclohexyl)carbamate

HRID 1592337
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인쇄 미리보기

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HRID 1592337 반응식
Cl.[F:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH2:9][CH:8]([NH2:13])[CH2:7][CH2:6]2.[CH:14]([C@@H:16]1[CH2:21][CH2:20][CH2:19][CH2:18][C@H:17]1[NH:22][C:23](=[O:32])[O:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=O.C(N(CC)CC)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[OH-].[Na+]>ClCCCl>[CH2:25]([O:24][C:23](=[O:32])[NH:22][C@@H:17]1[CH2:18][CH2:19][CH2:20][CH2:21][C@H:16]1[CH2:14][NH:13][CH:8]1[CH2:7][CH2:6][C:5]2[C:10](=[CH:11][CH:12]=[C:3]([F:2])[CH:4]=2)[CH2:9]1)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1
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참가 물질

7

반응물 5

HCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 5049666Sodium triacetoxyborohydrideHCID 196993636-Fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochlorideHCID 29923903Benzyl [(1r,2r)-2-formylcyclohexyl]carbamate

생성물 1

HCID 131726668
benzyl((1R,2S)-2-{[((2RS)-6-fluoro-1,2,3,4-tetrahydronaphthalen-2-yl)amino]methyl}cyclohexyl)carbamate
수율 69%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

A mixture of (RS)-(6-fluoro-1,2,3,4-tetrahydronaphthalen-2-yl)amine hydrochloride (200 mg, 0.99 mmol) and benzyl [(1R,2R)-2-formylcyclohexyl]carbamate (258 mg, 0.99 mmol) in 1,2-dichloroethane (4 mL) was treated with triethylamine (275 μL, 1.98 mmol) whereupon a clear solution resulted. Sodium triacetoxyborohydride (272 mg, 1.28 mmol) was added and the mixture was stirred at room temperature for 3.5 hours. Aqueous sodium hydroxide (1.0 N) was then added, and the mixture was extracted with ether. The organic phase was dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography, eluting with 5% methanol in dichloromethane, containing 0.5% aqueous ammonia, to provide a colorless oil (280 mg, 69%).

후처리

  1. customresulted
  2. extractionthe mixture was extracted with ether
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. concentrationconcentrated
  5. customThe residue was purified by flash column chromatography
  6. washeluting with 5% methanol in dichloromethane
  7. additioncontaining 0.5% aqueous ammonia

출처 및 근거

ORD 기록
ord-4ad87b87e83a4e578a618c6ed8b3d526
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07291744B2

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