Ethanol → HCID 69104602, compound

Participants

Reaction Conditions

Reaction Steps

Part A: To mixture of 345 mg (1.43 mmol) of 4-amino-N,N-dimethyl-N′-(methylsulfonyl)benzamidine, 1.5 mL of EtOH, and 0.5 mL of H2O heated at 100° C. was added portion-wise 311 mg (1.43 mmol) of 5-chloro-N-(oxiran-2-ylmethyl)thiophene-2-carboxamide. After 8 hours, the volatiles were evaporated and the compound purified by purified by ISCO System flash chromatography (Gradient elution 0% to 100% B over 40 min; (A=Hexane, B=AcOEt) then 0% to 100% B over 30 min; (A=AcOEt, B=5% MeOH and 1% NH4OH)) to yield 320 mg of N-(3-(4-(N,N-dimethyl -N′-(methylsulfonyl)carbamimidoyl)phenylamino)-2-hydroxypropyl)-5-chlorothiophene-2-carboxamide as a yellow oil. Further purification by prep HPLC yield an analytically pure sample. TR=4.758 min (Shimadzu Phenomenex S5 ODS 4.6×50 mm Luna flow rate 2.5 ml/mn; detection at 220 nM; gradient elution 0% to 100% B over 8 min; (A=10% MeOH, 90% H2O, 0.2% H3PO4 & B=90% MeOH, 10% H2O, 0.2% H3PO4). 1H NMR (500 MHz, CDCl3) δ 7.52 (d, J=4.05 Hz, 1H), 7.26 (d, J=8.05 Hz, 2H), 7.02 (d, J=4.05 Hz, 1H), 6.9 (d, J=8.05 Hz, 2H), 3.98 (m, 1H), 3.62 (t, 2H), 3.5 (m, 1H). 3.4 (m, 1H), 3.3 (m, 1H), 3.2 (m, 3H), 2.79 (s, 3H), 2.0 (m, 2H), 1.88 (m, 2H), ppm. LC-MS (ESI) 459.21 [M+H]+. HRMS (ESI) m/z calcd for C18H24N4O4S2Cl [M+H]+ 459.09276, found 459.0917.

Provenance & Evidence