Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063377Generated: November 1, 2026

Methanol → HCID 69783903, compound

https://huagongshe.com/reaction/1063377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Buten-1-amineHCID 30447—
ReactantHCID 69784064HCID 69784064—
ProductHCID 69783903HCID 6978390344%

Reaction Steps

300 mg (corresponds to 0.7 mmol) of crude 4-(5-Iodo-pent-1-ynyl)-piperidine-1-carboxylic acid 4-chloro-phenyl ester in 5 ml MeOH was treated with 0.7 ml (6.95 mmol) of N-methylallylamine (at 0° C.). The reaction was stirred overnight at room temperature and partitioned between aqueous 1N NaOH /ether (3×), the organic phases were dried (Na2SO4) and evaporated. Purification by flash-chromatography on silica gel (CH2Cl2/MeOH 19:1) gave 116 mg (44% over two steps) of 4-[5-(Allyl-methyl-amino)-pent-1-ynyl]-piperidine-1-carboxylic acid 4-chloro-phenyl ester, MS: 375 (MH+, 1Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964974B2
Source datasetuspto-grants-2005_11
ORD IDord-a789a9b4e1094345aec72906684adafc
Source noteuspto-grants-2005_11