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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705607Generated: October 30, 2026

Phenylacetyl chloride → HCID 11397684, compound

https://huagongshe.com/reaction/705607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 86611277HCID 86611277—
Solvent2-OxopropiononitrileHCID 69430—
ProductHCID 11397684HCID 1139768459%

Reaction Steps

6-(6,7-dimethoxy-quinolinyloxy)-5-fluoro-benzothiazol-2-ylamine (95 mg, 0.25 mmol), Et3N (0.10 ml, 0.72 mmol), phenylacetyl chloride (0.044 ml, 0.33 mmol), and THF (11.0 ml) were combined and stirred at room temperature for 1 hr. Additional phenylacetyl chloride (0.044 ml, 0.33 mmol) was added and the mixture heated to reflux for 1-2 hrs. After cooling to room temperature, the reaction mixture was diluted with 1:1 AcCN:H2O (11.0 ml) and the resulting solids filtered, washed with 1:1 AcCN:H2O and dried under high vacuum to give N-[6-(6,7-dimethoxy-quinolin-4-yloxy)-5-fluoro-benzothiazol-2-yl]-2-phenyl-acetamide (72 mgs, 59%). 1H-NMR (400 MHz, DMSO): 12.80 (s, 1H), 8.54 (d, 1H), 8.18 (d, 1H), 7.91 (d, 1H), 7.60 (s, 1H), 7.45 (s, 1H), 7.34 (m, 4H), 7.28 (m, 1H), 6.60 (d, 1H), 3.98 (s, 3H), 3.96 (s, 3H), 3.86 (s, 2H). LC/MS Calcd for [M+H]+ 490.1. found 490.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174947B2
Source datasetuspto-grants-2015_11
ORD IDord-12821a2027f34d9a9ae7d36b5485e8a3
Source noteuspto-grants-2015_11