Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372768Generated: November 2, 2026

Isoquinoline-1-carbaldehyde → HCID 58778962, compound

https://huagongshe.com/reaction/1372768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoquinoline-1-carbaldehydeHCID 265306—
ReactantIodo benzene diacetateHCID 12217721—
ReactantMethyl (4-amino-2-fluoro-3-hydroxyphenyl)acetateHCID 17859032—
SolventEthanolHCID 702—
ProductHCID 58778962HCID 5877896214.5%

Reaction Steps

In ethanol (13 ml), isoquinoline-1-carbaldehyde (500 mg, 3.18 mmol) and methyl 4-amino-2-fluoro-3-hydroxyphenylacetate (632 mg, 3.17 mmol) were stirred at room temperature for 2 days. Iodobenzene diacetate (1.23 g, 3.82 mmol) was added, and the reaction mixture was stirred at room temperature for 10 minutes. The reaction mixture was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane/ethyl acetate (3:1, v/v) eluate fractions, methyl (7-fluoro-2-(1-isoquinolinyl)-6-benzoxazolyl)acetate (155 mg, 14%) was obtained as a red brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-1012462665e0498394f4e929f9f7d78d
Source noteuspto-grants-2007_01