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Chemical Structure| 16406-00-1 Chemical Structure| 16406-00-1

Structure of 16406-00-1

Chemical Structure| 16406-00-1

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Product Details of [ 16406-00-1 ]

CAS No. :16406-00-1
Formula : C7H6N2OS
M.W : 166.20
SMILES Code : OCC1=CC=CC2=NSN=C21
MDL No. :MFCD02682036

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Application In Synthesis of [ 16406-00-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 16406-00-1 ]

[ 16406-00-1 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 16406-00-1 ]
  • [ 273749-25-0 ]
YieldReaction ConditionsOperation in experiment
96% aluminum nickel; In tetrahydrofuran; 2,3-Diaminobenzyl alcohol (2) Raney nickel (~5 g) was placed in a hydrogenation bottle and washed with THF three times before being slurried in 50 mL of THF. 4-Hydroxymethyl-2,1,3-benzothiadiazole56 (5.0 g, 30 mmol) was then added. It was hydrogenated under 10 psi pressure at room temperature for 6 hours. TLC was used to confirm that all starting material had been consumed. The reaction mixture was then filtered carefully through a pad of celite and washed with THF. After removal of the solvent, 2,3-diaminobenzyl alcohol (4.0 g, 96%) was obtained as a colorless crystalline solid. Rf=0.18 (hexane/ethyl acetate/MeOH=5:5:1); 1H NMR (200 MHz, DMSO) delta 4.33 (broad s, 2H), 4.36 (d, J=5.4 Hz, 2H), 4.43 (broad s, 2H), 4.96 (t, J=5.4 Hz, 1H), 6.43 (m, 3H); HRMS: Calcd. for C7H10N2O 138.0793, found 138.0830.
1.6 g With hydrogen; In methanol; at 20.0℃; for 16.0h; To a stirred solution of 2,l,3-benzothiadiazol-4-ylmethanol (2.5 g, 15 mmol) (from step 4) in methanol (150 mL) was added Raney nickel (100% w/w, washed five times with methanol) and it was hydrogenated under balloon pressure of hydrogen gas at ambient temperature. After 16 h, the reaction mixture was filtered through a celite bed and the residue was washed with methanol (3 x 250 mL). The combined filtrate was concentrated to afford (2, 3-diaminophenyl) methanol (1.6 g) as blue gum. NMR (400 MHz, DMSO-de) delta 6.48 (d, 1H, J = 7.20 Hz), 6.42 (d, 1H, J = 7.20 Hz), 6.36 (t, 1H, J = 7.20 Hz), 4.92 (bs, 1H), 4.43 (s, 2H), 4.35 (d, 4H, J = 14.80 Hz);
1.6 g With hydrogen; In methanol; at 20.0℃; for 16.0h; To a stirred solution of 2,l,3-benzothiadiazol-4-ylmethanol (2.5 g, 15 mmol) (from step 4) in methanol (150 mL) was added raney nickel (100% w/w, washed five times with methanol) and it was hydrogenated (under balloon pressure) at ambient temperature. After 16 h, the above reaction mass was filtered through a celite bed, the residue was washed with methanol (3 x 250 mL). The combined filtrate was concentrated to afford (2,3-diaminophenyl)methanol (1.6 g) as a gum. NMR (400 MHz, DMSO-de) delta 6.48 (d, IH, J=7.20 Hz), 6.42 (d, IH, J=7.20 Hz), 6.36 (t, IH, J = 7.20 Hz), 4.92 (br.s, IH), 4.43 (s, 2H), 4.35 (d, 4H, J = 14.80 Hz);MS: m/z 139 (M+l).
 

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