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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853858Generated: November 4, 2026

Boron tribromide → HCID 86689539, compound

https://huagongshe.com/reaction/1853858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 67450426HCID 67450426—
SolventDichloromethaneHCID 6344—
ProductHCID 86689539HCID 8668953979.1%

Reaction Steps

Following General Procedure F, tert-butyl 2-(2-chloro-4-(8-methoxy-4-oxo-4,5-dihydrothieno[2,3-c]quinolin-9-yl)phenyl)propylcarbamate (120 mg, 0.24 mmol) in CH2Cl2 at 0° C. was added BBr3 (1.0 M in CH2Cl2, 15 mL, 15 mmol) and the reaction was warmed to room temperature for 4 h. The reaction was quenched by pouring onto water or ice-water and the resulting mixture was concentrated and purified by preparatory HPLC (C18 silica, acetonitrile/water (with 0.05% TFA) gradient). The desired product was dissolved in aqueous HCl, concentrated and dried under high vacuum to afford the desired product as a brown solid (40 mg, 43%): 1H NMR (500 MHz, CD3OD) δ 7.65 (ddd, J=9.9, 9.3, 6.1 Hz, 2H), 7.46-7.36 (m, 2H), 7.33-7.27 (m, 1H), 7.18 (t, J=9.0 Hz, 1H), 6.10 (dd, J=28.8, 5.4 Hz, 1H), 3.86-3.66 (m, 1H), 3.29-3.12 (m, 2H), 1.44-1.28 (m, 3H); ESI MS m/z 385 [C20H17ClN2O2S+H]+; HPLC >99% (AUC), tR=9.07 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962648B2
Source datasetuspto-grants-2015_02
ORD IDord-1f7ba51bf8ca4ebfa61be735d90e380a
Source noteuspto-grants-2015_02