HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895556Generated: November 1, 2026
HCID 66888570, compound → HCID 49854432, compound
https://huagongshe.com/reaction/1895556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66888570 | HCID 66888570 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 49854432 | HCID 49854432 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513433B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-c5a9c6c47317470ba9b1213761d12adf |
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| Source note | uspto-grants-2013_08 |
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