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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66310Generated: October 29, 2026

Piperidin-4-ol → Hpr 611

https://huagongshe.com/reaction/66310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
ReactantSodiumHCID 5360545—
ReactantMethyl 2-oxo-5-chloro-3-benzothiazolineacetateHCID 13040939—
SolventMethanolHCID 887—
SolventSodium MethoxideHCID 10942334—
ProductHpr 611HCID 308245380.8%

Reaction Steps

4-Hydroxypiperidine (47.2 g) was added at room temperature to and dissolved in a methanolic sodium methoxide solution prepared from sodium metal (2.2 g) in dry methanol (100 ml). To the resultant solution was added methyl 5-chloro-2-oxo-3-benzothiazolineacetate (100 g), and the mixture was heated for 3 hours under reflux with stirring. The reaction mixture was left to cool, poured into ice water (500 ml) and stirred for 30 minutes. The precipitates were collected, washed with water and then dried to give 3-(4-hydroxypiperidino)carbonylmethyl-5-chloro-2-benzothiazolinone (102.5 g), which was recrystallized from 90% aqueous methanol to give colorless crystals, m.p. 180.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04131681
Source datasetuspto-grants-1978_12
ORD IDord-96b26f98857542468026d27821d2f913
Source noteuspto-grants-1978_12