HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751743Generated: October 26, 2026
4-Methylmorpholine → HCID 59753639, compound
https://huagongshe.com/reaction/751743
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Ethanone, 2-amino-1-phenyl-, hydrochloride (1:1) | HCID 2723597 | — |
| Reactant | 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride | HCID 2734059 | — |
| Reactant | 5-Cyano-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid | HCID 59753518 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59753639 | HCID 59753639 | — |
Reaction Steps
To a solution of 5-cyano-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid (Preparation 62, 0.035 g, 0.19 mmol) in THF (15 mL) under argon was added 2-aminoacetophenone hydrochloride (0.036 g, 0.21 mmol), N-methylmorpholine (25 μM, 0.23 mmol) and DMTMM (0.072 g, 0.27 mmol). The reaction mixture was stirred at rt for 16 h. The reaction mixture was concentrated to dryness in vacuo. The residue was partitioned between ethyl acetate (100 mL) and water (50 mL). The organic phase was separated and the aqueous phase was further extracted with ethyl acetate (100 mL). The combined organic extract was washed with 1N NaOH (40 mL), saturated sodium chloride (40 mL), dried (MgSO4), filtered and concentrated in vacuo. Crude material was purified by chromatography in hexane/ethyl acetate (1:2) and recrystallised from methanol to give the title compound. m/z (ES+)=304 [M+H]+; RT=4.37.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405210B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-27eb160ed24d4c229b38e3acb0a1d037 |
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| Source note | uspto-grants-2008_07 |
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