HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502552Generated: October 27, 2026
Methylamine → N2-(2-(benzo[d]isothiazol-3-ylamino)ethyl)-N5-methylpyridine-2,5-dicarboxamide
https://huagongshe.com/reaction/502552
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | 6-(2-(Benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)nicotinic acid | HCID 11856361 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N2-(2-(benzo[d]isothiazol-3-ylamino)ethyl)-N5-methylpyridine-2,5-dicarboxamide | HCID 11854748 | — |
Reaction Steps
A mixture of 6-(2-(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)nicotinic acid (62 mg, 0.13 mmol), diethyl cyanophosphonate (21 μL, 0.14 mmol), methylamine (2.0M soln in THF, 15 μL, 0.14 mmol) and triethylamine (20 μL, 0.14 mmol) in dichloromethane (5 mL) was allowed to stir at room temperature overnight. The solution was washed with water, then dried over anhydrous sodium sulfate, filtered and the filtrate concentrated under reduced pressure. Purification by column chromatography, on silica gel, eluting with a mixture of 30% ethyl acetate in hexanes, and selected fractions were combined and concentrated under reduced pressure to yield N2-(2-(benzo[d]isothiazol-3-ylamino)ethyl)-N5-methylpyridine-2,5-dicarboxamide as a white solid, (50 mg). 1H NMR (300 MHz, DMSO-d6): 9.16 (broad s, 1H), 8.99 (s, 1H), 8.79 (m, 1H), 8.37 (d, 1H), 8.23 (t, 2H), 7.91 (d, 1H), 7.58 (s, 1H), 7.49 (t, 1H), 7.39 (t, 1H), 3.61 (m, 3H), 3.34 ppm (m, 4H). MW=355 confirmed by LC-MS, tr=2.98 min (Method B) MH+=356.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776847B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-a9b115221f64481baf29217314fb1032 |
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| Source note | uspto-grants-2010_08 |
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