HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784093Generated: October 30, 2026
2,4,6-Trichlorobenzoyl chloride → HCID 11465112, compound
https://huagongshe.com/reaction/1784093
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trichlorobenzoyl chloride | HCID 2733703 | — |
| Reactant | HCID 57591096 | HCID 57591096 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 11465112 | HCID 11465112 | 24% |
Reaction Steps
To a suspension of 2-amino-9-methoxy-6,7-dihydro-pyrimido[6,1-a]isoquinolin-4-one (7) (40 mg, 0.16 mmol) in CHCl3 (3 mL), DMAP (30.1 mg, 0.24 mmol) and 2,4,6-trichlorobenzoyl chloride (37.5 uL, 0.24 mmol) was added and stirred at 25° C. overnight. After cooling, the mixture was purified on BondElut® SCX (Varian Incorporated) then column chromatography on silica gel (CHCl3/MeOH=50/1 as eluant) to give the title compound (17.1 mg, 24%). 1H-NMR (400 MHz, CDCl3) δ 7.90 (d, 1H), 7.42 (s, 2H), 6.95 (dd, 1H), 6.82 (d, 1H), 4.27 (t, 2H), 3.90 (s, 3.17) and 3.03 (t, 2H); MS (ESI) (M+H)+ 449.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501512B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-108e0b8006264da1af16c9338792a540 |
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| Source note | uspto-grants-2009_03 |
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