HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689728Generated: November 1, 2026
Bis(2-Methoxyethyl)amine → HCID 16049333, compound
https://huagongshe.com/reaction/1689728
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(2-Methoxyethyl)amine | HCID 2383 | — |
| Reactant | Ethyl 2-amino-8-(pentafluoroethyl)-3H-1-benzazepine-4-carboxylate | HCID 15953875 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 16049333 | HCID 16049333 | — |
Reaction Steps
Trimethylaluminuni (0.34 mL of a 2.0 M solution in toluene) was added to bis(2-methoxyethyl)amine (92 mg, 0.69 mmol) in DCE (3 mL). After 10 minutes solid (1E,4E)-ethyl 2-amino-8-(perfluoroethyl)-3H-benzo[b]azepine-4-carboxylate (80 mg, 0.23 mmol) was added and the vessel was sealed and heated to 75° C. for 16-20 hours. Upon cooling the reaction was quenched with saturated Rochelle's salt (2 mL) and after 20 minutes the mixture was partitioned between CH2Cl2 (50 mL) and brine (50 mL). The phases were separated and the aqueous was extracted with CH2Cl2 (2×20 mL). The combined organics were dried and concentrated. The crude material was purified via preparative TLC (2, 0.5 mm plates, eluting with 5-10% MeOH/CH2Cl2 with 4-6 drops of NH4OH). 1H NMR (CDCl3) δ 2.81 (s, 2H), 3.36 (s, 6H), 3.55-3.74 (m, 8H), 6.98 (s, 1H), 7.20 (d, 1H), 7.40 (d, 1H), 7.39 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153622B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-8db7985bd8e04c08983896c3be88da2d |
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| Source note | uspto-grants-2012_04 |
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