Ammonium Hydroxide → (R)-tert-butyl 2-(5-methoxycarbonylthiophen-2-yl)pyrrolidine-1-carboxylate

HRID 564219

반응식

HRID 564219 반응식
[C:1]([N:8]1[CH2:12][CH2:11][CH2:10][CH2:9]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].C1C[C@H]2N(C[C@H]3[C@@H]4CCCCN4C[C@@H]2C3)CC1.C([Li])(CC)C.Br[C:36]1[S:40][C:39]([C:41]([O:43][CH3:44])=[O:42])=[CH:38][CH:37]=1.F[B-](F)(F)F.C(P(C(C)(C)C)C(C)(C)C)(C)(C)C.[OH-].[NH4+]>COC(C)(C)C.C1CCCCC1.CCOCC.[Cl-].[Zn+2].[Cl-].C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:44][O:43][C:41]([C:39]1[S:40][C:36]([C@H:12]2[CH2:11][CH2:10][CH2:9][N:8]2[C:1]([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2])=[CH:37][CH:38]=1)=[O:42]

참가 물질

12

실험 절차

To a solution of N-Boc-pyrrolidine (3 mL) and (−)-sparteine (3.9 mL) in tert-butyl methyl ether (36 mL) at −78° C. was added 1.4M sec-butyl lithium in cyclohexane (12.21 mL). The solution was stirred for 3 hours and 1M zinc chloride in ether (10.2 mL) was added. The mixture was stirred for 30 minutes and warmed to ambient temperature for 30 minutes. Methyl 5-bromothiophene-2-carboxylate (3.15 g), tri-tert-butylphosphine tetrafluoroborate (249 mg) and palladium(II) acetate (153 mg) were added, and the mixture was stirred at ambient temperature overnight, treated with concentrated ammonium hydroxide (1 mL) and stirred for 30 minutes, and filtered through diatomaceous earth (Celite®). The filtrate was washed with 0.5M hydrochloric acid solution and water and concentrated. The concentrate was flash chromatographed on silica gel with ethyl acetate/hexane.

후처리

  1. stirringThe mixture was stirred for 30 minutes
  2. stirringthe mixture was stirred at ambient temperature overnight
  3. stirringstirred for 30 minutes
  4. filtrationfiltered through diatomaceous earth (Celite®)
  5. washThe filtrate was washed with 0.5M hydrochloric acid solution and water
  6. concentrationconcentrated
  7. customchromatographed on silica gel with ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-6c310ccc24894e758f571d8f23d9781f
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08067613B2

연결된 노트

불러오는 중…