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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457189Generated: October 30, 2026

Potassium Carbonate → 2-(5-{3-[3-(4-Chloro-benzyloxy)-pyrrolidin-1-yl]-propylidene}-5,11-dihydro-10-oxa-1-aza-dibenzo[a,d]cyclohepten-7-yl)-propan-2-ol

https://huagongshe.com/reaction/457189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(E)-2-[5-(3-bromo-propylidene)-5,11-dihydro-10-oxa-1-aza-dibenzo[a,d]cyclohepten-7-yl]-propan-2-olHCID 23136844—
Reactant(R)-3-(4-chloro-benzyloxy)-pyrrolidineHCID 53765332—
SolventAcetonitrile--water (1/1)HCID 18373917—
Product2-(5-{3-[3-(4-Chloro-benzyloxy)-pyrrolidin-1-yl]-propylidene}-5,11-dihydro-10-oxa-1-aza-dibenzo[a,d]cyclohepten-7-yl)-propan-2-olHCID 66758641—

Reaction Steps

To a solution of (R)-3-(4-chloro-benzyloxy)-pyrrolidine (0.88 mmol, 2.0 eq) in acetonitrile:water (4:1) was added potassium carbonate (0.88 mmol, 2.0 eqv) and (E)-2-[5-(3-bromo-propylidene)-5,11-dihydro-10-oxa-1-aza-dibenzo[a,d]cyclohepten-7-yl]-propan-2-ol and the resulting mixture was stirred at room temperature for 24 h. The reaction mixture was concentrated in vacuo, diluted with ethyl acetate, and dried over sodium sulfate. The crude product was purified by Reverse Phase HPLC. 1H-NMR (CDCl3) δ: 1.40 (6H, s), 1.15–1.35 (1H, m), 1.85–2.05 (1H, m), 2.20–2.40 (1H, m), 2.35–2.65 (8H, m), 3.90–4.10 (1H, m), 4.30–4.50 (2H, d), 5.10–5.30 (2H, br, s), 6.05 (1H, t), 6.50 (1H, dd), 7.10–7.50 (4H, m), 7.70 (1H, dd), 8.50 (1H, dd). ESI-MS m/z: 505 (M+1), UV retention time: 1.52 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186729B2
Source datasetuspto-grants-2007_03
ORD IDord-d42906e75ed3444aa5615e02ee2ba56f
Source noteuspto-grants-2007_03