HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733679Generated: October 27, 2026
Ethylmorpholine → HCID 57840793, compound
https://huagongshe.com/reaction/733679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-Aminomethyltetrahydropyran | HCID 2773210 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 7-chloro-1H-pyrrolo[2,3-c]pyridine-4-carboxylic acid | HCID 57840843 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57840793 | HCID 57840793 | 56.6% |
Reaction Steps
To a solution of 7-chloro-1H-pyrrolo[2,3-c]pyridine-4-carboxylic acid (110 mg) in dimethylformamide (4 ml) was added 4-ethylmorpholine (187 μl), tetrahydro-pyran-4-ylmethylamine (97 mg), 1-hydroxybenzotriazole hydrate (118 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (129 mg) and the solution stirred at room temperature overnight. The dimethylformamide was evaporated and the residue dissolved in ethyl acetate (10 ml). The organic layer was then washed with 5% sodium hydrogen carbonate solution (4 ml) and brine (4 ml). The organic layer was dried (MgSO4) and evaporated to give a pale orange solid. The solid was triturated with diethyl ether and then filtered off, sucked dry then dried at 40° C. under vacuum to afford the title compound (93 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589206B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-3edbe2e917894c798517cf8153eeef79 |
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| Source note | uspto-grants-2009_09 |
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