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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491012Generated: October 29, 2026

Pyridine → HCID 86596236, compound

https://huagongshe.com/reaction/491012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 86596235HCID 86596235—
ProductHCID 86596236HCID 8659623682%

Reaction Steps

A solution of N -[2-(2-bromoethylcarbamylthio)benzoyl]-β-alaninamide (0.37 g, 1.0 mmol) in pyridine (5 ml) was stirred for 8 h under nitrogen. The pyridine was removed in vacuo, and the crude product was purified by column chromatography on silica using chloroform-methanol(7:3 v/v) as eluent. Yield: 82%. 1H NMR (DMSO-d6): 2.38(t, 2H, CH2), 3.40(q, 2H, CH2), 3.72(q,2H, CH2), 4.72(t, 2H, CH2), 6.92(brs, 1H, NH2), 7.36-7.58(m, 5H, Ar—H, NH2), 8.26(t, 2H, Py-H), 8.36(t, 1H, NH), 8.66(t, 1H, Py-H), 9.12(d, 2H, Py-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528274B2
Source datasetuspto-grants-2009_05
ORD IDord-4385f05f04d54160be625e620474cf35
Source noteuspto-grants-2009_05