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Tris(2-carboxyethyl)phosphine → Dansyl-cystamine maleimide

HRID 929393
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 929393
[S:1]([N:17](S(C1C2C=CC=C(N(C)C)C=2C=CC=1)(=O)=O)[CH2:18][CH2:19][S:20][S:21][CH2:22][CH2:23][NH2:24])([C:4]1[C:16]2[CH:15]=[CH:14][CH:13]=[C:9]([N:10]([CH3:12])[CH3:11])[C:8]=2[CH:7]=[CH:6][CH:5]=1)(=[O:3])=[O:2].C(C(O)=O)CP(CCC(O)=O)CCC(O)=O.Br[C:58]1[C:59]([NH:61][C:62](=[O:64])[CH:63]=1)=[O:60]>CO>[S:1]([NH:17][CH2:18][CH2:19][S:20][S:21][CH2:22][CH2:23][NH2:24])([C:4]1[C:16]2[CH:15]=[CH:14][CH:13]=[C:9]([N:10]([CH3:12])[CH3:11])[C:8]=2[CH:7]=[CH:6][CH:5]=1)(=[O:2])=[O:3].[C:59]1(=[O:60])[NH:61][C:62](=[O:64])[CH:63]=[CH:58]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 119411Tris(2-carboxyethyl)phosphineHCID 118195503-bromo-2,5-dihydro-1H-pyrrole-2,5-dioneHCID 86668292Di-dansyl cystamine

Produkt 1

HCID 86668295Dansyl-cystamine maleimideAusbeute 94,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel2×

Versuchsvorschrift

A round bottomed flask was charged with di-dansyl cystamine (100 mg, 0.16 mmol), TCEP (46 mg, 1 eq), and MeOH (10 ml). The reaction mixture was stirred at ambient temperature under argon for 3 hrs. Bromomaleimide (56 mg, 2 eq) in MeOH (5 ml), was added to the reaction mixture. After 16 hrs, the reaction mixture was concentrated in vacuo. The residue was worked up with DCM and brine. The organic layers were combined, dried (MgSO4) and purified by flash chromatography (silica gel, 0-30% EtOAC-CHCl3) to yield the desired compound (73 mg, 55%). 1HNMR (CDCl3, 600 MHz), δ8.5 (1H, d J 8.5 Hz aromatic H's), δ8.2 (2H, m aromatic H's), δ8.1 (1H, s CONH), δ7.5 (2H, m, aromatic H's), δ7.15 (1H, d, J=7.5 Hz aromatic H's), δ6.0 (1H, s, CO2CH) δ5.89 (1H, t, J 6.4 SO2NH), δ3.20 (2H, q, J 6.7 NHCH2), δ3.99 (2H, t, J 6.9 SCH2), δ2.86 (6H, s NCH3); 13CNMR (CDCl3, 150 MHz), 6169.6, 168.0, 152.0, 150.7, 134.4, 131.0, 129.9, 129.7, 129.5, 128.8, 123.4, 119.3, 118.7, 115.6, 45.5, 41.0, 31.8; IR (cm−1) 3277 (br) 1720 (s) MS (ES−) m/z relative intensity: 404 (M, 100); Exact mass calculated for [C18H18N3O4S2] requires m/z 404.0739. Found 404.0733.

Aufarbeitung

  1. waitAfter 16 hrs
  2. concentrationthe reaction mixture was concentrated in vacuo
  3. dry with materialdried (MgSO4)
  4. custompurified by flash chromatography (silica gel, 0-30% EtOAC-CHCl3)

Quellen und Nachweise

ORD-Eintrag
ord-63ad4eb0dde2472c9ae062712402014f
Quelldatensatz
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09295729B2

Notizen zur Reaktion

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