Ammonia → 5-(5-Bromopentyl)-1,3,4-thiadiazol-2-amine

6-Bromohexanoic acid (5.35 g, 27.4 mmol), concentrated sulphuric acid (15 mL), and thiosemicarbazide (3.0 g, 32.9 mmol) were slowly heated to 80-90° C. for 12 h. After cooling, the content was poured onto crushed ice. The mixture was neutralized with 10% aqueous ammonia and extracted with ethyl acetate (3×100 mL). The organic extracts were washed with 10% Na2CO3 (2×50 mL), water (100 mL), and brine (100 mL), dried over Na2SO4, filtered, and concentrated. The residue was purified by chromatography over silica gel 60 (70-230 mesh) eluted with CH2Cl2:MeOH 19:1 to give the product as a solid, mp 128-130° C., in 59% yield (4.03 g, 16.2 mmol). 1H NMR (300 MHz, CDCl3) δ 1.51-1.60 (m, 2), 1.71-1.79 (m, 2), 1.81-1.92 (m, 2), 2.92 (t, 2, J=7.5 Hz), 3.40 (t, 2, J=6.9 Hz), 5.33 (s, 2); 13C NMR (75 MHz, CDCl3) δ 26.9, 28.1, 29.3, 31.8, 35.0, 158.1, 168.2; HRMS (ESI+, m/z) calculated for C7H13BrN3S 250.0014. observed 250.0005 (M+H)+.

1. temperatureAfter cooling
2. additionthe content was poured
3. customonto crushed ice
4. extractionextracted with ethyl acetate (3×100 mL)
5. washThe organic extracts were washed with 10% Na2CO3 (2×50 mL), water (100 mL), and brine (100 mL)
6. dry with materialdried over Na2SO4
7. filtrationfiltered
8. concentrationconcentrated
9. customThe residue was purified by chromatography over silica gel 60 (70-230 mesh)
10. washeluted with CH2Cl2:MeOH 19:1

ORD record

ord-f609be36bbdb4bfd98c20625c672b8ce

Source dataset

uspto-grants-2016_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09320734B2