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Dimethyl Sulfoxide → HCID 131722001, 화합물

HRID 1954031
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HRID 1954031 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH3:11][CH2:12][C@H:13]1[C:43](=[O:44])[CH2:42][C@H:41]([OH:45])[C@@H:40]([CH3:46])[C@@H:39](/[C:47](/[CH3:58])=[CH:48]/[C@H:49]2[CH2:54][C@@H:53]([O:55][CH3:56])[C@H:52]([OH:57])[CH2:51][CH2:50]2)[O:38][C:36](=[O:37])[C@H:35]2[N:30]([CH2:31][CH2:32][CH2:33][CH2:34]2)[C:28](=[O:29])[C:26](=[O:27])[C@:24]2([OH:59])[O:25][C@@H:20]([C@@H:21]([O:61][CH3:62])[CH2:22][C@H:23]2[CH3:60])[C@@H:19]([O:63][CH3:64])[CH2:18][C@@H:17]([CH3:65])[CH2:16][C:15]([CH3:66])=[CH:14]1.C(N(CC)CC)C>C(Cl)Cl.CCOCC>[CH2:12]([C@@H:13]1[CH:14]=[C:15]([CH3:66])[CH2:16][C@H:17]([CH3:65])[CH2:18][C@H:19]([O:63][CH3:64])[C@H:20]2[O:25][C@:24]([OH:59])([C@H:23]([CH3:60])[CH2:22][C@@H:21]2[O:61][CH3:62])[C:26](=[O:27])[C:28](=[O:29])[N:30]2[C@@H:35]([CH2:34][CH2:33][CH2:32][CH2:31]2)[C:36](=[O:37])[O:38][C@H:39](/[C:47](/[CH3:58])=[CH:48]/[C@@H:49]2[CH2:50][CH2:51][C:52](=[O:57])[C@H:53]([O:55][CH3:56])[CH2:54]2)[C@H:40]([CH3:46])[C@@H:41]([OH:45])[CH2:42][C:43]1=[O:44])[CH3:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 5282071Ascomycin

생성물 1

HCID 131722001HCID 131722001, 화합물수율 59.5%

시약·촉매·용매 2

HCID 3283
Diethyl Ether
용매
HCID 6344Dichloromethane용매2회

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온도
-70 °C

실험 절차

Methylsulfide-chlorine complex was prepared by adding oxalyl chloride (0.32 g) into a solution of dimethylsulfoxide (0.44 g) in 4 mL of methylene chloride and stirred at -70° C. for 30 minutes. The solution of the complex was slowly added to a stirred solution of ascomycin (1.6 g) in 5 mL of methylene chloride at -70° C. After stirring for 30 minutes, triethylamine (1.4 g) was added and the mixture was allowed to stir for an additional 30 minutes at -70° C. The reaction mixture was then allowed to warm to room temperature followed by additional stirring for 1 hour. The reaction mixture was diluted with 100 mL of ether, washed with 1N-HCl aq. solution (30 mL×2), brine (30 mL), dried over magnesium sulfate anhydrous, and the solvent removed in vacuo. The crude product was purified on 70 gram of silica gel, eluting with ether to obtain 0.95 g of the title compound.

후처리

  1. customMethylsulfide-chlorine complex was prepared
  2. stirringAfter stirring for 30 minutes
  3. stirringto stir for an additional 30 minutes at -70° C
  4. temperatureto warm to room temperature
  5. stirringby additional stirring for 1 hour
  6. washwashed with 1N-HCl aq. solution (30 mL×2), brine (30 mL)
  7. dry with materialdried over magnesium sulfate anhydrous
  8. customthe solvent removed in vacuo
  9. customThe crude product was purified on 70 gram of silica gel
  10. washeluting with ether

출처 및 근거

ORD 기록
ord-6848ebff6d534c9fb21533654e1fa263
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06121257

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