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Potassium Carbonate → (Z)-((2-((2-(dimethylamino)ethyl)thio)acetyl)azanediyl)bis(ethane-2,1-diyl) dioleate

HRID 1471454
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HRID 1471454 반응식
OC(C(F)(F)F)=O.[C:8]([O:27][CH2:28][CH2:29][NH:30][CH2:31][CH2:32][O:33][C:34](=[O:52])[CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41]/[CH:42]=[CH:43]\[CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH3:51])(=[O:26])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]/[CH:16]=[CH:17]\[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].C([O-])([O-])=O.[K+].[K+].[CH3:59][N:60]([CH3:68])[CH2:61][CH2:62][S:63][CH2:64][C:65](O)=[O:66].CCN=C=NCCCN(C)C.Cl>C(Cl)Cl.CN(C1C=CN=CC=1)C.CO.O>[C:8]([O:27][CH2:28][CH2:29][N:30]([C:65](=[O:66])[CH2:64][S:63][CH2:62][CH2:61][N:60]([CH3:68])[CH3:59])[CH2:31][CH2:32][O:33][C:34](=[O:52])[CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41]/[CH:42]=[CH:43]\[CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH3:51])(=[O:26])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]/[CH:16]=[CH:17]\[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]
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참가 물질

9

반응물 4

HCID 11430Potassium CarbonateHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 167927492-{[2-(Dimethylamino)ethyl]sulfanyl}acetic acidHCID 131732750(Z)-azanediylbis(ethane-2,1-diyl) dioleate TFA salt2회

생성물 1

HCID 72550488(Z)-((2-((2-(dimethylamino)ethyl)thio)acetyl)azanediyl)bis(ethane-2,1-diyl) dioleate

시약·촉매·용매 4

HCID 142844-(Dimethylamino)pyridine촉매HCID 887Methanol용매HCID 962Water용매HCID 6344Dichloromethane용매

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온도
2.5 °C

실험 절차

Synthesis of (Z)-azanediylbis(ethane-2,1-diyl) dioleate TFA salt previously described. (Z)-azanediylbis(ethane-2,1-diyl) dioleate TFA salt (4.06 g, 6.41 mmol) was stirred in DCM (60 mL) with 10% K2CO3 (30 mL) at 0-5° C. After 30 min, the organic phase was separated and the aqueous phase was further extracted with DCM (30 mL). The combined organic phases were stirred with anhydrous MgSO4 for a period of 30 minutes at 0-5° C., filtered, and washed with DCM (30 mL). To the combined filtrates were added to 2-((2-(dimethylamino)ethyl)thio)acetic acid (1.26 g, 7.70 mmol), EDC HCl salt (1.84 g, 9.62 mmol), DMAP (78.3 mg, 0.64 mmol). The thin suspension was stirred overnight at room temperature; after which a period of time, the solution became clear. Next day, deionized water (60 mL) and methanol (30 mL) were added. After stirring for 10 minutes, the clear organic layer was isolated. The turbid aqueous phase is extracted with DCM. The combined organic extracts were concentrated. Crude material was filtered through a plug of silica and taken up in DCM (40 mL) and PBS (pH=11, 50 mL) was added. The mixture was stirred at room temperature for 10 min. Then, the organic phase was separated and the aqueous phase is extracted again with DCM (15 mL). The combined organic phases were stirred with anhydrous MgSO4 for a period of 30 min. The mixture was then filtered, and washed with DCM. The combined filtrates were concentrated in vacuo to yield (Z)-((2-((2-(dimethylamino)ethyl)thio)acetyl)azanediyl)bis(ethane-2,1-diyl) dioleate (3.44 g).

후처리

  1. customthe organic phase was separated
  2. extractionthe aqueous phase was further extracted with DCM (30 mL)
  3. filtrationfiltered
  4. washwashed with DCM (30 mL)
  5. stirringThe thin suspension was stirred overnight at room temperature
  6. stirringAfter stirring for 10 minutes
  7. customthe clear organic layer was isolated
  8. extractionThe turbid aqueous phase is extracted with DCM
  9. concentrationThe combined organic extracts were concentrated
  10. filtrationCrude material was filtered through a plug of silica
  11. additionPBS (pH=11, 50 mL) was added
  12. stirringThe mixture was stirred at room temperature for 10 min
  13. customThen, the organic phase was separated
  14. extractionthe aqueous phase is extracted again with DCM (15 mL)
  15. stirringThe combined organic phases were stirred with anhydrous MgSO4 for a period of 30 min
  16. filtrationThe mixture was then filtered
  17. washwashed with DCM
  18. concentrationThe combined filtrates were concentrated in vacuo

출처 및 근거

ORD 기록
ord-4b6da5269c7c4947b97ea1ca5210b458
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09011903B2

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