Acetic Anhydride → 3-(tert-Butoxycarbonylamino)-1-(2-phenyl-1,3-dithiaN-2-yl)cyclohexyl acetate

HRID 530856노트

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HRID 530856 반응식
[C:1]1([CH:7]2[S:12][CH2:11][CH2:10][CH2:9][S:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([N-]C(C)C)(C)C.[Li+].C1C[O:24][CH2:23][CH2:22]1.CCCCCCC.C(C1C=CC=CC=1)C.[O:41]=[C:42]1[CH2:47][CH2:46][CH2:45][CH:44]([NH:48][C:49](=[O:55])[O:50][C:51]([CH3:54])([CH3:53])[CH3:52])[CH2:43]1.C(OC(=O)C)(=O)C>C1COCC1.O>[C:23]([O:41][C:42]1([C:7]2([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[S:8][CH2:9][CH2:10][CH2:11][S:12]2)[CH2:47][CH2:46][CH2:45][CH:44]([NH:48][C:49]([O:50][C:51]([CH3:52])([CH3:54])[CH3:53])=[O:55])[CH2:43]1)(=[O:24])[CH3:22]

참가 물질

8

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온도
-20 °C

실험 절차

To a solution of 2-phenyl-1,3-dithiane (12 mmol, 2.35 g) in THF (15 mL) at 78° C. was added a solution of lithium diisopropylamide in THF/heptane/ethylbenzene (12 mmol, 1.8 M, 6.7 mL) under argon. The reaction mixture was warmed up to −20° C. and stirred for 30 minutes at −20° C. The reaction mixture was cooled down to −78° C. tert-Butyl 3-oxocyclohexylcarbamate (5 mmol, 1.065 g) in THF was added. The reaction mixture was allowed to warm up to room temperature and stirred for overnight. Acetic anhydride (20 mmol, 1.9 mL) was added. The reaction mixture was stirred at room temperature for 4 hours. Water was added. The organics were extracted with EtOAc. 3-(tert-Butoxycarbonylamino)-1-(2-phenyl-1,3-dithiaN-2-yl)cyclohexyl acetate was obtained after purification by silica gel column chromatography.

후처리

  1. additionwas added
  2. temperatureto warm up to room temperature
  3. stirringstirred for overnight
  4. stirringThe reaction mixture was stirred at room temperature for 4 hours
  5. extractionThe organics were extracted with EtOAc

출처 및 근거

ORD 기록
ord-4a1af14b5b734e9facdf6a7847e6fe81
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09351965B2

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