HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263752Generated: October 29, 2026
Trimethylsilyl iodide → 4-Amino-1,4-dihydroisoquinolin-3(2H)-one
https://huagongshe.com/reaction/1263752
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 12593302 | HCID 12593302 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Amino-1,4-dihydroisoquinolin-3(2H)-one | HCID 22312038 | — |
Reaction Steps
Step D—Removal of the Methoxyoxycarbonyl Group (MOC): To the 4-methoxycarbonylamino-1,2,3,4-tetrahydroisoquinoline-3-one (3.4 mmoles) in 30 mL of acetonitrile was added 2 mole equivalents of trimethylsilyliodide (TMSI). The reaction mixture was heated to 50-80° C. for 3 hrs and then cooled and poured into a seperatory funnel. The reaction mixture was diluted with ethyl acetate and washed with 1 molar K2CO3 and then with 5% NaHSO3. The organic layer was dried over Na2SO4 and filtered. The solvent was removed under reduced pressure to give the 4-amino-1,2,3,4-tetrahydroisoquinoline-3-one derivative. Typical yields range from 50-87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06541466B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-8902e2db87f7403d897a3a5ecc8695e4 |
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| Source note | uspto-grants-2003_04 |
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