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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393532Generated: October 29, 2026

Hydrochloric Acid → HCID 12069228, compound

https://huagongshe.com/reaction/393532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant6-Bromo-2-(methylthio)oxazolo[5,4-b]pyridineHCID 12069221—
ReactantHCID 178418997HCID 178418997—
ProductHCID 12069228HCID 1206922864%

Reaction Steps

The title compound was prepared from 6-bromo-2-methylsulfanyl-oxazolo[5,4-b]pyridine (prepared from 5-bromo-2-hydroxy-3-nitropyridine by the methods described in Examples 4, 5 and 7) by the procedure described in Example 9 in 64% yield: 1H NMR (CDCl3, 400 MHz) δ 7.90 (d, 1H, J=2.1 Hz), 7.59 (d, 1H, J=2.1 Hz), 4.50-4.49 (m, 1h), 3.91 (t, 2H, J=5.8 Hz), 3.18-3.11 (m, 4H), 3.03-2.96 (m, 2H), 2.16-2.08 (m, 2H), 1.85-1.76 (m, 2H); 13C NMR (CDCl3, 100 MHz) δ 161.4, 138.8, 125.3, 121.4, 116.7, 116.2, 57.0, 50.6, 46.4, 44.3, 26.8; MS (Cl) m/z 323.0 (M+1); HPLC retention time=3.08 min. The hydrochloride salt was prepared by diluting in ethyl acetate and adding a 2.5 N HCl solution in ethyl acetate: mp>300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809094B2
Source datasetuspto-grants-2004_10
ORD IDord-c2687c40d75346869d14dcd6e2722954
Source noteuspto-grants-2004_10