isothiocyanatomethylcyclopropane

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound was prepared from 2-amino-5-chlorobenzenesulfonamide and cyclopropylmethyl isothiocyanate by a method analogous to the one described in Example 4; m.p. 288-290° C. (ethyl acetate); 1H-NMR (DMSO-d6): δ 0.20-0.54 (m, 4H, CH2CH2), 1.05 (m, 1H, CH), 3.10 (distorted t, 1H, NHCH2), 7.22 (d, 1H, ArH), 7.31 (br., 1H, NH), 7.55-7.69 (m, 2H, ArH), 10.7 (br.s, 1H, NH); MS: m/e 285/287 (M+); (C11H12N3Cl1O2S1) calc. C, 46.24; H, 4.23; N, 14.71; found C, 46.48; H, 4.32; N, 14.72.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound was prepared from 2-amino-5-chlorobenzenesulfonamide and cyclopropylmethyl isothiocyanate by a method analogous to the one described in Example 4; m.p. 288-290° C. (ethyl acetate); 1H-NMR (DMSO-d6): δ 0.20-0.54 (m, 4H, CH2CH2), 1.05 (m, 1H, CH), 3.10 (distorted t, 1H, NHCH2), 7.22 (d, 1H, ArH), 7.31 (br., 1H, NH), 7.55-7.69 (m, 2H, ArH), 10.7 (br.s, 1H, NH); MS: m/e 285/287 (M+); (C11H12N3Cl1O2S1) calc. C, 46.24; H, 4.23; N, 14.71; found C, 46.48; H, 4.32; N, 14.72.

Conditions: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of (isothiocyanatomethyl)cyclopropane (3.3 g, 31.13 mmol) (J. Org. Chem., 1972, 37, 1162-1168) and acetonitrile (4 ml) was dissolved in dry THF (50 ml) and cooled to −78° C. under a nitrogen atmosphere. A solution of sodium bis(trimethylsilyl)amide in THF (1.0M, 66 ml, 66 mmol) was added over 10 min and the reaction mixture then allowed to warm to r.t. over 2 h. EtOH (50 ml) and N,N-dimethyluracil (4.8 g, 34.2 mmol) were added and the mixture heated to reflux for 24 h. The mixture was cooled and concentrated in vacuo. The residue was dissolved in acetonitrile (50 ml) and bromonitromethane (7.30 g, 46.7 mmol) was added. The mixture was heated to 55° C. for 18 h then cooled to r.t. and diluted with ice/water (100 ml). The resulting solid was isolated by filtration to give the title compound as a brown solid (3.3 g, 40%). δH (CDCl3) 7.52 (1H, d, J 9.6 Hz), 6.87 (2H, br s), 6.58 (1H, d, J 9.6 Hz), 3.96 (2H, d, J 7.2 Hz), 1.40-1.33 (1H, m), 0.62-0.51 (4H, m). LCMS (ES+) RT 2.92 minutes, 266.0 (M+H)+. to warm to r.t. over 2 h the mixture heated to reflux for 24 h The mixture was cooled concentrated in vacuo The residue was dissolved in acetonitrile (50 ml) The mixture was heated to 55° C. for 18 h then cooled to r.t. The resulting solid was isolated by filtration

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound was prepared from 2-amino-5-chlorobenzenesulfonamide and cyclopropylmethyl isothiocyanate by a method analogous to the one described in Example 4; m.p. 288-290° C. (ethyl acetate); 1H-NMR (DMSO-d6): δ 0.20-0.54 (m, 4H, CH2CH2), 1.05 (m, 1H, CH), 3.10 (distorted t, 1H, NHCH2), 7.22 (d, 1H, ArH), 7.31 (br., 1H, NH), 7.55-7.69 (m, 2H, ArH), 10.7 (br.s, 1H, NH); MS: m/e 285/287 (M+); (C11H12N3Cl1O2S1) calc. C, 46.24; H, 4.23; N, 14.71; found C, 46.48; H, 4.32; N, 14.72.