Triethylamine → Tricyclo[3.3.1.13,7]dec-2-yl (+/-)-[2-[[2-(benzo[b]thien-3-yl)ethyl]amino]-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl]carbamate

HRID 1198074

Reaktionsgleichung

Reaktionsgleichung von HRID 1198074
[CH:1]12[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH:2]1[O:11][C:12]([NH:14][C:15]([CH3:29])([C:26](O)=[O:27])[CH2:16][C:17]1[C:25]3[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=3)[NH:19][CH:18]=1)=[O:13])[CH2:8]2.O.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.Cl.[NH2:54][CH2:55][CH2:56][C:57]1[C:58]2[CH:65]=[CH:64][CH:63]=[CH:62][C:59]=2[S:60][CH:61]=1.CCN(CC)CC>CN(C=O)C>[S:60]1[CH:61]=[C:57]([CH2:56][CH2:55][NH:54][C:26](=[O:27])[C:15]([NH:14][C:12](=[O:13])[O:11][CH:2]2[CH:1]3[CH2:10][CH:5]4[CH2:6][CH:7]([CH2:9][CH:3]2[CH2:4]4)[CH2:8]3)([CH2:16][C:17]2[C:25]3[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=3)[NH:19][CH:18]=2)[CH3:29])[C:58]2[CH:65]=[CH:64][CH:63]=[CH:62][C:59]1=2

Komponenten

7

Edukt 5

HCID 8471TriethylamineHCID 209554Benzo(b)thiophene-3-ethylamine, hydrochlorideHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 148025032-adamantyloxycarbonyl-alpha-methyl-DL-tryptophan

Produkt 1

HCID 86747493Tricyclo[3.3.1.13,7]dec-2-yl (+/-)-[2-[[2-(benzo[b]thien-3-yl)ethyl]amino]-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl]carbamate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

A solution of 0.50 g (1.26 mmol) of 2-adamantyloxycarbonyl-α-methyl-DL-tryptophan and 0.18 g (1.33 mmol) of 1-hydroxybenzotriazole hydrate in 8 mL of anhydrous DMF (under a N2 atmosphere) was treated in one portion with 0.27 g (1.41 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride. The mixture was stirred at room temperature for 2 hours, treated with 0.30 g (1.40 mmol) of 3-[2-aminoethyl)benzo[b]thiophene hydrochloride plus 0.25 mL (0.18 g, 1.79 mmol) of Et3N, and stirred for an additional 18 hours. The reaction mixture was partitioned between 100 mL of EtOAc and 150 mL of H2O. The layers were separated and the aqueous layer extracted with fresh EtOAc (3×75 mL). The combined organic layers were washed with 5% aqueous citric acid (3×150 mL), brine (1×150 mL), 5% aqueous NaHCO3 (3×150 mL), and brine again. The organic layer was dried (Na2SO4) and evaporated (vacuum) to an off-white foam. The residue was chromatographed (230-400 mesh SiO2 in a 21×300 mm column, eluted with 2% MeOH in CH2Cl2) to yield the purified product as a white foam, 0.40 g (57%); 1H NMR (CDCl3) δ 1.47-1.92 (17H, m), 2.92 (2H, t, J 7 Hz), 3.25 (1H, d, J 15 Hz), 3.46-3.57 (3H, m), 4.79 (1H, br s), 5.14 (1H, br s), 6.27 (1H, m), 7.02 (2H, m), 7.11-7.86 (8H, m), 8.10 (1H, br s).

Aufarbeitung

  1. stirringstirred for an additional 18 hours
  2. customThe reaction mixture was partitioned between 100 mL of EtOAc and 150 mL of H2O
  3. customThe layers were separated
  4. extractionthe aqueous layer extracted with fresh EtOAc (3×75 mL)
  5. washThe combined organic layers were washed with 5% aqueous citric acid (3×150 mL), brine (1×150 mL), 5% aqueous NaHCO3 (3×150 mL), and brine again
  6. dry with materialThe organic layer was dried (Na2SO4)
  7. customevaporated (vacuum) to an off-white foam
  8. customThe residue was chromatographed (230-400 mesh SiO2 in a 21×300 mm column
  9. washeluted with 2% MeOH in CH2Cl2)

Quellen und Nachweise

ORD-Eintrag
ord-7ffe8b6d526b46c8b2b625b18caae238
Quelldatensatz
uspto-grants-1994_01
Patentnummer
US05278316

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