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Home > Encyclopedia > Fmoc-Sec(Mob)-OH, Fmoc-Sec(pMeOBzl)-OH...

Fmoc-Sec(Mob)-OH, Fmoc-Sec(pMeOBzl)-OH...

Fmoc-Sec(Mob)-OH, Fmoc-Sec(pMeOBzl)-OH... structure

Fmoc-Sec(Mob)-OH, Fmoc-Sec(pMeOBzl)-OH... 

structure

Fmoc-Sec(Mob)-OH, Fmoc-Sec(pMeOBzl)-OH... Basic Attributes

510.459

511.089783

Characteristics

84.9

4.78040

382.3±32.9 °C

Drug Information

Fmoc-Sec(MBzl)-OH

Fmoc-Sec(Mob)-OH, Fmoc-Sec(pMeOBzl)-OH... Use and Manufacturing

A mixture of 14 (790 mg, 1.5mmol) and trimethyltin hydroxide (989 mg, 5.5 mmol) was dissolved in dry 1, 2‐dichloroethane (15 mL). Afterstirring overnight at 35°C, the mixture was filtered, and the filtrate was evaporated. The resulting crudeproduct was purified by silica gel column chromatography (hexane:EtOAc = 2:1 to 0:1) to give 15 as a colorlessoil or white solid (702 mg, 91percent). The spectral data of 15 were identical to the literature.37 The purity wasconfirmed by 1H NMR and HPLC. 1H NMR (CDCl3): H 2.98 (2H, m, βH), 3.78 (3H, s, p‐OMe), 3.79 (2H, s, CH2), 4.26 (1H, t, JHH 6.8 Hz, Fmoc‐CH), 4.45 (1H, d, JHH 6.7 Hz, Fmoc‐CH2), 4.70 (1H, m, αH), 5.54 (1H, d, JHH 7.8 Hz, NH), 6.83 (2H, d, JHH 8.4 Hz, ArH), 7.20 (2H, d, JHH 8.3 Hz, ArH), 7.33 (2H, m, ArH), 7.42 (2H, m, ArH), 7.63 (2H, t, JHH 6.7 Hz, ArH), 7.78 (2H, m, ArH). 13C NMR (CDCl3): C 25.1, 27.7, 47.1, 53.6, 55.3, 67.3, 114.1, 120.0, 125.1, 127.1, 127.8, 130.0, 141.3, 143.6, 158.7. 77Se NMR (CDCl3): Se 216.7.

Computed Properties

Molecular Weight:510.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:10
Exact Mass:511.08979
Monoisotopic Mass:511.08979
Topological Polar Surface Area:84.9
Heavy Atom Count:33
Complexity:631
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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