Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-Methoxyethyl)amineHCID 2383—
ReactantEthyl 2-amino-8-(pentafluoroethyl)-3H-1-benzazepine-4-carboxylateHCID 15953875—
Solvent1,2-DichloroethaneHCID 11—
SolventTolueneHCID 1140—
ProductHCID 16049333HCID 16049333—

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153622B2
Source datasetuspto-grants-2012_04
ORD IDord-8db7985bd8e04c08983896c3be88da2d
Source noteuspto-grants-2012_04