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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242776Generated: October 30, 2026

Hydrochloric Acid → HCID 21060089, compound

https://huagongshe.com/reaction/1242776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant(3S)-2-((tert-butoxy)carbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 664088—
ReactantN-(3-dimethylaminopropyl)-N'-ethylcarbodiimide methyliodideHCID 10236463—
ReactantHCID 21060090HCID 21060090—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 21060089HCID 21060089152.1%
ProductHCID 69078990HCID 69078990—

Reaction Steps

tert-Butyl 3-(N-{(1R)-1-[(4-chlorophenyl)methyl]-2-oxo-2-(4-(2-pyridyl)piperazinyl)ethyl}carbamoyl)(3S)-1,2,3,4-tetrahydroisoquinoline-2-carboxylate was prepared from N-{(1R)-1-[(4-chlorophenyl)methyl]-2-oxo-2-(4-(2-pyridyl)piperazinyl)ethyl}(tert-butoxy)-carboxamide (Step 1) (800 mg, 1.80 mmol), following the procedure for Example 93, Step 2 using 25 mL of EtOAc satd with HCl for the first step, and DIEA (240 μl, 1.38 mmol), Boc-L-Tic-OH (340 mg, 1.2 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide methiodide (740 mg, 2.5 mmol), HOAT (184 mg, 1.35 mmol) and DMF (15 mL) for the second step. The crude was purified by flash chromatography (SiO2, 1:1, hexane:EtOAc) to yield the title compound (460 mg). MS (ESI, pos. ion) m/z: 604 (M+H), (ESI, neg. ion) m/z: 602 (M−H). Calc'd for C33H38ClN5O4: 604.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115607B2
Source datasetuspto-grants-2006_10
ORD IDord-639db3f79b564561a8d633788657e7c2
Source noteuspto-grants-2006_10