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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264582Generated: October 31, 2026

Triethylamine → HCID 86618289, compound

https://huagongshe.com/reaction/2264582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
Reactant7-Methoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepine hydrochlorideHCID 12234840—
ReactantAP-24592HCID 46838908—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 86618289HCID 86618289—

Reaction Steps

586 mg (1.97 mMol) triphosgene are dissolved in 70 ml ice-cooled CH2Cl2. Then a solution of 1618 mg (5.92 mMol) 3-trifluoromethyl-4-(4-methylpiperazin-1-ylmethyl)-aniline and 1.179 ml (8.46 mMol) Et3N in 12 ml CH2Cl2 is added during 11 min. After 3 additional minutes, the mixture is warmed up to rt by a water bath and then a solution of 1.00 g (5.64 mMol) of 7-methoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepine [Monatsheft Chemie, 97 (1966), 150] and 786 μl (5.64 mMol) Et3N in 18 ml CH2Cl2 is added during 10 min. After 2 h at rt, the mixture is diluted with water and EtOAc, the aqueous phase separated off and extracted twice with EtOAc. The organic layers are washed with water and brine, dried (Na2SO4) and concentrated. Column chromatography (SiO2; EtOAc/EtOH/NH3conc. 95:5:1→90:10:1) gives the title compound: MS: [M+1]+=477; HPLC: AtRet=12.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855215B2
Source datasetuspto-grants-2010_12
ORD IDord-fcfb836f124e4428af6a589b440e361b
Source noteuspto-grants-2010_12