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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895556Generated: November 1, 2026

HCID 66888570, compound → HCID 49854432, compound

https://huagongshe.com/reaction/1895556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66888570HCID 66888570—
SolventAcetic AcidHCID 176—
ProductHCID 49854432HCID 49854432—

Reaction Conditions

Temperature120 °C

Reaction Steps

Step-5: A solution of benzyl 3-((2-amino-3-carbamoylphenyl)carbamoyl)-3-methyl-3,4-dihydroisoquinoline-2(1H)-carboxylate (40 mg, 0.087 mmol) in acetic acid (2 ml) was heated to 80° C. and stirred overnight. The reaction was further heated to 120° C. for 3 h. The reaction mixture was concentrated, neutralized with aq. NaHCO3 and extracted with ethyl acetate. The ethyl acetate layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. Purification of the crude product by preparative TLC using hexane/ethyl acetate (1:1) mixture as eluent afforded benzyl 3-(4-carbamoyl-1H-benzo[d]imidazol-2-yl)-3-methyl-3,4-dihydroisoquinoline-2(1H)-carboxylate. MS (ES+): m/z 441.22 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513433B2
Source datasetuspto-grants-2013_08
ORD IDord-c5a9c6c47317470ba9b1213761d12adf
Source noteuspto-grants-2013_08