HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23686Generated: October 28, 2026
Diisopropylethylamine → HCID 10311790, compound
https://huagongshe.com/reaction/23686
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide | HCID 22574363 | — |
| Reactant | 1-(6-Methoxypyridin-3-yl)-2-(methylamino)ethanol dihydrochloride | HCID 22574369 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10311790 | HCID 10311790 | 63.6% |
Reaction Steps
A mixture of N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide (100 mg, 0.25 mmol), 1-(6-methoxypyridin-3-yl)-2-(methylamino)ethanol dihydrochloride (Preparation 52) (97 mg, 0.38 mmol) and diisopropylethylamine (199 μL, 1.2 mmol) in dry DMF (5 mL) was heated to 60° C., becoming a solution. The reaction was stirred for 6 hours at that temperature. After cooling to room temperature, the solution was diluted with water (15 mL). The resulting milky suspension was stirred vigorously for 30 minutes, and then left standing overnight at room temp. The mixture was filtered, and the collected solid was washed with water and dried in vacuo, leaving a white solid. Recrystallization from acetonitrile (10 mL, dissolved with warming and then cooled to 0° C. overnight) gave the title compound (86 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852731B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-9a38a45072e2457dadf539f7f9ca3d9c |
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| Source note | uspto-grants-2005_02 |
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