Réaction #491389

ord-dedb5cf989484f619f2f87e0ec309baf

Équation de réaction

NCC(O)c1ccccc1
2-amino-1-phenyl-ethanol
CN(C)c1ccc(CNC(=O)NCCCC(=O)NO)cc1
Compound 2
CN(C)c1ccc(CNC(=O)NCCCC(=O)NO)cc1
4-[3-(4-Dimethylamino-benzyl)-ureido]-N-hydroxy-butyramide
Cc1ccc(S(=O)(=O)O)cc1.NCCC(=O)OCc1ccccc1
3-amino-propionic acid benzyl ester toluene-4-sulfonic acid
CN(C)c1ccc(CN)cc1.Cl.Cl
4-dimethylaminobenzylamine dihydrochloride
O=C(CCNC(=O)NCC(O)c1ccccc1)NO
Compound 14
O=C(CCNC(=O)NCC(O)c1ccccc1)NO
N-hydroxy-3-[3-(2-hydroxy-2-phenyl-ethyl)-ureido]-propionamide

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

Compound 14 was prepared using the methodology described for the preparation of Compound 2, by substituting 4-amino-butyric acid benzyl ester toluene-4-sulfonic acid with 3-amino-propionic acid benzyl ester toluene-4-sulfonic acid and 4-dimethylaminobenzylamine dihydrochloride with 2-amino-1-phenyl-ethanol. 1H NMR (CD3OD) δ 7.40-7.22 (m, 5H), 4.69 (dd, J=7.8, 4.2 Hz, 1H), 3.41-3.34 (m, 3H), 3.22 (dd, J=13.8, 7.8 Hz, 1H), 2.25 (t, J=6.9 Hz, 2H). 13C NMR (CD3OD) δ 171.1, 161.3, 144.2, 129.5, 128.7, 127.3, 74.6, 48.9, 37.5, 34.7.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08748463B2uspto-grants-2014_06