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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602275Generated: October 30, 2026

71034-40-7 → HCID 59684236, compound

https://huagongshe.com/reaction/602275

Reaction equation

Participants

RoleNameHCIDCharge
Reactant71034-40-7HCID 4962722—
ReactantHCID 59684264HCID 59684264—
ProductHCID 59684236HCID 5968423694%

Reaction Conditions

Temperature120 °C

Reaction Steps

A neat mixture of 3-(4-fluoro-3-methoxyphenyl)-7-(4-methoxybenzyloxy)isochromen-1-one (100 mg, 0.25 mmol) and 2-amino-N-tert-butyl acetamide (INTERMEDIATE I.2) (32 mg, 2.46 mmol) was heated at 120° C. for 3 h. The reaction mixture was cooled and partitioned between ethyl acetate and sat. NH4Cl (aq.). The organic layer was washed with brine (1×20 mL), dried (MgSO4) and concentrated in vacuo to afford N-tert-butyl-2-(3-(4-fluoro-3-methoxyphenyl)-7-(4-methoxybenzyloxy)-1-oxo-1H-isoquinolin-2-yl)acetamide (120 mg, 0.23 mmol, 94%) which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906504B2
Source datasetuspto-grants-2011_03
ORD IDord-aeab2679d0594bc0bdb351a1ea1e4fe7
Source noteuspto-grants-2011_03