HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11386720, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Butanesulfonyl chloride | HCID 75430 | — |
| Reactant | (4-Methanesulfonyl-phenyl)-[5-nitro-6-(piperidin-4-yloxy)-pyrimidin-4-yl]-amine | HCID 11257886 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11386720 | HCID 11386720 | — |
Reaction Steps
Compound A29 was prepared in a similar manner as described above using (4-methanesulfonyl-phenyl)-[5-nitro-6-(piperidin-4-yloxy)-pyrimidin-4-yl]-amine (i.e., Compound A2) (15 mg, 0.035 mmol), triethylamine (20 μl), butane-1-sulfonyl chloride (8 mg, 0.056 mmol), DMF (0.6 mL), 1H NMR (CDCl3, 400 MHz) δ 0.98 (t, 3H), 1.51 (m, 2H), 1.83 (m, 2H), 2.07 (m, 4H), 2.97 (m, 2H), 3.08 (s, 3H), 3.40 (m, 2H), 3.58 (m, 2H), 5.68 (m, 1H), 7.87 (d, 2H), 7.98 (d, 2H), 8.41 (s, 1H), 10.21 (s, 1H). Exact mass calculated for C20H27N5O7S2 513.14, found 514.4 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07838525B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-4d04a5d25edd4f738da3bcca82251d4e |
| Source note | uspto-grants-2010_11 |