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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33325Generated: October 26, 2026

1-(4-Bromophenethyl)pyrrolidine → HCID 22266698, compound

https://huagongshe.com/reaction/33325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenethyl)pyrrolidineHCID 12177810—
Reactant2-[4-(2-Diethylamino-ethyl)-phenyl]-3,4,5,6-tetrahydro-azepino[5,4,3-cd]indol-6-oneHCID 22266679—
ProductHCID 22266698HCID 22266698—

Reaction Steps

In a manner similar to that described for 2-[4-(2-diethylamino-ethyl)-phenyl]-3,4,5,6-tetrahydro-azepino[5,4,3-cd]indol-6-one (Example YY), the tricyclic bromide (198 mg, 0.75 mmol) and 1-[2-(4-bromo-phenyl)-ethyl]-pyrrolidine were coupled to yield 2-[4-(2-pyrrolidin-1-yl-ethyl)-phenyl]-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one, 160 mg (59%) as a beige solid: m.p. 228-229° C. (dec); 1H NMR (300 MHz, d6-DMSO) δ 1.69 (m, 4H), 2.51 (m, 4H), 2.67 (m, 2H), 2.81 (m, 2H), 3.05 (m, 2H), 3.39 (m, 2H), 7.20 (t, J=7.8 Hz, 1H), 7.39 (d, J=8.1 Hz, 2H), 7.56 (m, 3H), 7.68 (d, J=7.5 Hz, 1H), 8.08 (br t, 1H), 11.31 (br s, 1H). MS (FAB, MH+): 360. Anal. (C23H25N3O) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429578B2
Source datasetuspto-grants-2008_09
ORD IDord-4096601ba2ed4bdd9b68429745d01bc5
Source noteuspto-grants-2008_09