HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Hydroxybenzotriazole → HCID 68328437, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | HCID 68328124 | HCID 68328124 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68328437 | HCID 68328437 | 29.2% |
Reaction Steps
To a solution of 5-(5-(5-(isopropylamino)-1,3,4-oxadiazol-2-yl)-1-tosyl-1H-indol-3-yl)nicotinic acid (500 mg, 0.967 mmol) in DMF (10 mL) was added PyBOP (755 mg, 1.45 mmol), HOBt (196 mg, 1.45 mmol) and DIPEA (0.50 mL, 2.9 mmol). Methylamine hydrochloride (77.7 mg, 1.160 mmol) was added and the reaction was stirred for 2 h under Ar at RT. The reaction was quenched with water (200 mL) to get a brown precipitate. The precipitate was filtered, washed with water (2×100 mL) and dried. The crude product was purified with basic alumina chromatography (eluting with EtOAc) to give 5-(5-(5-(isopropylamino)-1,3,4-oxadiazol-2-yl)-1-tosyl-1H-indol-3-yl)-N-methylnicotinamide (150 mg, 29%). MS (ESI, pos. ion) m/z: 531.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321756B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-fc8a363b407a40598bdba52e066f1691 |
| Source note | uspto-grants-2016_04 |