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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849392Generated: October 27, 2026

2,3,4,5-Tetrahydro-1-(1-naphthalenylcarbonyl)-1h-1,4-benzodiazepine → HCID 178478880, compound

https://huagongshe.com/reaction/849392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4,5-Tetrahydro-1-(1-naphthalenylcarbonyl)-1h-1,4-benzodiazepineHCID 10566283—
Reactant7-Bromo-2,3,4,5-tetrahydro-1-(1H-imidazol-4-ylmethyl)-4-(1-naphthalenylcarbonyl)-1H-1,4-benzodiazepine, hydrochlorideHCID 178479667—
ReactantHCID 178479669HCID 178479669—
SolventDichloromethaneHCID 6344—
ProductHCID 178478880HCID 178478880—

Reaction Steps

Example 42 was prepared as an off white solid from 7-bromo-1,4-benzodiazepine (prepared as described in Compound B of Example 11) using the following procedure: Compound A of Example 4; Compound B of Example 4; Compound C of Example 4; Compound D of Example 1, using methylene chloride as solvent, purification by prep HPLC (YMC S5 ODS 30×250 mm; gradient elution with 0 to 100% buffer B over 45 min; buffer A=MeOH:H2O:TFA (10:90:0.1); buffer B=MeOH:H2O:TFA (90:10:0.1); 25 mL/min) and conversion to the HCl salt by lyophilization from 1M HCl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011029
Source datasetuspto-grants-2000_01
ORD IDord-c987e10a173f4e0e9a851a42ceb04421
Source noteuspto-grants-2000_01