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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242726Generated: November 1, 2026

1,2-Dichloroethane → methyl 2-{4-[(2R)-2-({(3S)-2-[(tert-butyl)oxycarbonyl](3-1,2,3,4-tetrahydroisoquinolyl)}carbonylamino)-3-(4-chlorophenyl)propanoyl]piperazinyl}benzoate

https://huagongshe.com/reaction/1242726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant(3S)-2-((tert-butoxy)carbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 664088—
ReactantMethyl 2-{4-[(2r)-2-amino-3-(4-chlorophenyl)propanoyl]piperazinyl}-benzoate hydrochlorideHCID 69074691—
Productmethyl 2-{4-[(2R)-2-({(3S)-2-[(tert-butyl)oxycarbonyl](3-1,2,3,4-tetrahydroisoquinolyl)}carbonylamino)-3-(4-chlorophenyl)propanoyl]piperazinyl}benzoateHCID 58714303—

Reaction Steps

The title compound was prepared according to the procedure described in Preparation V by using methyl 2-{4-[(2R)-2-amino-3-(4-chlorophenyl)propanoyl] piperazinyl}-benzoate hydrochloride (2.6 g, 5.9 mmol), Boc-L-Tic-OH (Bachem) (1.8 g, 6.5 mmol), HOAT (Aldrich) (810 mg, 5.9 mmol), and EDC (Aldrich) (2.3 g, 12 mmol) and DIEA (Aldrich) (1.0 mL, 5.9 mmol). The title compound was isolated and purified by column chromatography (CH2Cl2 with 1.5% NH3 2M in MeOH) (2.8 g). MS (ESI, pos. ion) m/z: 661 (M+H). Calc'd for C36H41ClN4O6: 660.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115607B2
Source datasetuspto-grants-2006_10
ORD IDord-fb9029a9a0fb4af7af89d5bca8b566c8
Source noteuspto-grants-2006_10