HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748294Generated: October 30, 2026
Triethylamine → ethyl 4,4-difluoro-1-oxo-2,3,4,5-tetrahydro-1H-[1,4]diazepino[1,2-a]indole-8-carboxylate
https://huagongshe.com/reaction/1748294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | diethyl 1-(3-amino-2,2-difluoropropyl)-1H-indole-2,6-dicarboxylate | HCID 67235788 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 4,4-difluoro-1-oxo-2,3,4,5-tetrahydro-1H-[1,4]diazepino[1,2-a]indole-8-carboxylate | HCID 67235837 | 70% |
Reaction Steps
To a solution of diethyl 1-(3-amino-2,2-difluoropropyl)-1H-indole-2,6-dicarboxylate (2.3 g) in ethanol (160 mL) are added triethylamine (2.7 mL, 19.0 mmol) and K2CO3 (1.3 g, 9.5 mmol). The mixture is heated at 80° C. for 16 h. Ethanol is removed under vacuum and water (100 mL) is added. The resulting light yellow solid is filtered and dried to afford the title compound (1.2 g, 70% for 3 steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150577B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-53a90e529eb14dd1abcc102a91bb120b |
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| Source note | uspto-grants-2015_10 |
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