Oxalic Acid → 1[n-[(1,3-Benzodioxol-5-yl)sulfonyl]-n-(2-methylpropyl)amino]-3(s)-[bis(phenylmethyl)amino]-4-phenyl-2(r)-butanol

HRID 8848

반응식

HRID 8848 반응식
[C:1]1([CH2:7][N:8]([C@@H:16]([CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C@H:17]([OH:24])[CH2:18][NH:19][CH2:20][CH:21]([CH3:23])[CH3:22])[CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(O)(=O)C(O)=O.C(=O)([O-])[O-].[K+].[K+].[O:44]1[C:48]2[CH:49]=[CH:50][C:51]([S:53](Cl)(=[O:55])=[O:54])=[CH:52][C:47]=2[O:46][CH2:45]1>O.O1CCOCC1.C(OCC)(=O)C>[O:44]1[C:48]2[CH:49]=[CH:50][C:51]([S:53]([N:19]([CH2:18][C@@H:17]([OH:24])[C@@H:16]([N:8]([CH2:9][C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH2:7][C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[CH2:25][C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[CH2:20][CH:21]([CH3:23])[CH3:22])(=[O:54])=[O:55])=[CH:52][C:47]=2[O:46][CH2:45]1

참가 물질

8

반응물 4

HCID 971Oxalic AcidHCID 11430Potassium CarbonateHCID 49134011,3-Benzodioxole-5-sulfonyl chlorideHCID 9806223N-(3(S)-[N,N-bis(phenylmethyl)amino]-2(R)-hydroxy-4-phenylbutyl]-N-isobutylamine

생성물 1

HCID 113878411[n-[(1,3-Benzodioxol-5-yl)sulfonyl]-n-(2-methylpropyl)amino]-3(s)-[bis(phenylmethyl)amino]-4-phenyl-2(r)-butanol수율 105%

시약·촉매·용매 3

HCID 962Water용매2회HCID 8857Ethyl Acetate용매HCID 312751,4-Dioxane용매2회

실험 절차

To a 5000 mL, 3-necked flask fitted with a mechanical stirrer was added N-[3(S)-[N,N-bis(phenylmethyl)amino]-2(R)-hydroxy-4-phenylbutyl]-N-isobutylamine.oxalic acid salt (354.7 g, 0.7 mole) and 1,4-dioxane (2000 mL). A solution of potassium carbonate (241.9 g, 1.75 moles) in water (250 mL) was then added. The resultant heterogeneous mixture was stirred for 2 hours at room temperature followed by the addition of 1,3-benzodioxole-5-sulfonyl chloride (162.2 g, 0.735 mole) dissolved in 1,4-dioxane (250 mL) over 15 minutes. The reaction mixture was stirred at room temperature for 18 hours. Ethyl acetate (1000 mL) and water (500 mL) were charged to the reactor and stirring continued for another 1 hour. The aqueous layer was separated and further extracted with ethyl acetate (200 mL). The combined ethyl acetate layers were washed with 25% brine solution (500 mL) and dried over anhydrous magnesium sulfate. After filtering and washing the magnesium sulfate with ethyl acetate (200 mL), the solvent in the filtrate was removed under reduced pressure yielding the desired sulfonamide as an viscous yellow foamy oil (440.2 g 105% yield). HPLC/MS (electrospray) (m/z 601 [M+H]+].

후처리

  1. customTo a 5000 mL, 3-necked flask fitted with a mechanical stirrer
  2. stirringThe reaction mixture was stirred at room temperature for 18 hours
  3. stirringstirring
  4. waitcontinued for another 1 hour
  5. customThe aqueous layer was separated
  6. extractionfurther extracted with ethyl acetate (200 mL)
  7. washThe combined ethyl acetate layers were washed with 25% brine solution (500 mL)
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationAfter filtering
  10. washwashing the magnesium sulfate with ethyl acetate (200 mL)
  11. customthe solvent in the filtrate was removed under reduced pressure

출처 및 근거

ORD 기록
ord-3b114308753546f9ba44edcd7d8e73f8
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07091219B2

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