Dimethyl Sulfoxide → Phenylmethyl 2-formyl-2,3-dihydro-1H-indole-1-carboxylate

HRID 484405노트

반응식

HRID 484405 반응식
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH2:11]([O:18][C:19]([N:21]1[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[CH2:23][CH:22]1[CH2:30][OH:31])=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(N(CC)CC)C>C(Cl)Cl.O>[CH2:11]([O:18][C:19]([N:21]1[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[CH2:23][CH:22]1[CH:30]=[O:31])=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

참가 물질

7

반응물 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 2776402Benzyl 2-(Hydroxymethyl)-1-Indolinecarboxylate

생성물 1

HCID 19795226Phenylmethyl 2-formyl-2,3-dihydro-1H-indole-1-carboxylate

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매2회

실험 절차

Dimethyl sulfoxide (2.75 ml) is added to a solution of oxalyl chloride (1.7 ml) in methylene chloride (45 ml) at -78° under nitrogen via cannula over six minutes. After 20 minutes, (±) 1-benzyloxycarbonyl-2-hydroxymethylindoline (IV, EXAMPLE 4, 5.003 g) in methylene chloride (20 ml) is added via cannula over 12 minutes. The mixture is stirred for 30 minutes, then triethyl amine (7.40 ml) is added. The mixture is stirred at -78° for an additional 20 minutes then stirred at 20°-25° for one hour, then poured into water (50 ml) and the layers are separated. The aqueous layer is extracted with methylene chloride (5×20 ml). The combined organic layers are washed sequentially with saline, hydrochloric acid (3N, 100 ml), water (100 ml), aqueous sodium carbonate (5%, 100 ml) and again with water (100 ml). The organic layer is then dried over magnesium sulfate and concentrated under reduced pressure to give an oil. The oil is passed over a silica column (27.5 cm×4.0 cm, 40-63 mm) and is eluted with ethyl acetate/hexane (1/5.6 300 ml, 1/42 1), collecting 29 ml fractions. The appropriate fractions are pooled and concentrated to give the title compound, NMR (CDCl3, 300 MHz), 9.62, 7.93, 7.34, 7.20, 7.11, 6.97, 5.23, 4.82, 3.36 and 3.13 δ; CMR (CDCl3, 75.47 MHz) 29.74, 65.76, 67.57, 115.05, 123.34, 124.64, 128.08, 128.20, 128.40, 128.61, 135.57, 141.7, 151.9 and 198.73 δ; IR (CHCl3) 2940, 1700, 1600, 1480, 1400, 1320, 1270-1190 and 1030 cm-1 ; MS (m/e) 281, 252, 208, 117, 91 and 65, exact mass calcd for C17H15NO3 (281.1052), found 281.1066; TLC (ethyl acetate/hexane, 1/3) Rf =0.28.

후처리

  1. stirringThe mixture is stirred at -78° for an additional 20 minutes
  2. stirringthen stirred at 20°-25° for one hour
  3. customthe layers are separated
  4. extractionThe aqueous layer is extracted with methylene chloride (5×20 ml)
  5. washThe combined organic layers are washed sequentially with saline, hydrochloric acid (3N, 100 ml), water (100 ml), aqueous sodium carbonate (5%, 100 ml) and again with water (100 ml)
  6. dry with materialThe organic layer is then dried over magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customto give an oil
  9. washis eluted with ethyl acetate/hexane (1/5.6 300 ml, 1/42 1)
  10. customcollecting 29 ml fractions
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-7b0ce3acfedd4b7f9362d502a5831e28
출처 데이터셋
uspto-grants-1993_07
특허 번호
US05231188

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