Triethylamine → N-BOC-S-trityl-cysteine 4-amino-3-methoxybenzoyl methionine methyl ester

N-BOC-S-trityl-cysteine (0.76 g, 1.74 mmol) in dry THF (27.5 ml) was reacted with Et3N (0.24 ml), IBCF (0.23 ml, 1.74 mmol) at -10° C. as described above. HCl-4-amino-3-methoxybenzoyl methionine methyl ester (0.55 g, 1.58 mmol) in dry CH2Cl2 (8.7 ml) with Et3N (0.30 ml) was added to the mixture and was allowed to stir overnight under nitrogen. It was worked up as described for N-BOC-S-trityl-cysteine-4-aminobenzoyl methionine methyl ester in Example 1, and the crude material was chromatographed on silica gel using a 2:1 mixture of hexanes and ethyl acetate to give 0.18 g (15.2%) of pure product. 1H NMR (CDCl3) 1.45 (9 H, s), 2.05-2.33 (5 H, m), 2.57-2.65 (2 H, m), 2.68-2.72 (1 H, m), 2.75-2.96 (1 H, m), 3.78 (3 H, s), 3.84 (3 H, s), 4.90-5.00 (1 H, m), 5.03-5.18 (1 H, m), 7.17-7.48 (17 H, m), 8.30-8.38 (1 H, m), 8.65 (1 H, br s).

1. customthe crude material was chromatographed on silica gel using
2. additiona 2:1 mixture of hexanes and ethyl acetate

ORD-Eintrag

ord-b6c98498f04f4bc9948f88a0116f0de7

Quelldatensatz

uspto-grants-1998_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05834434