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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244461Generated: October 30, 2026

HCID 44236097, compound → HCID 66958890, compound

https://huagongshe.com/reaction/1244461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 44236097HCID 44236097—
ReactantHCID 178478989HCID 178478989—
SolventDiethyl EtherHCID 3283—
ProductHCID 66958890HCID 66958890—

Reaction Steps

Prepared using the same method as for Intermediate I-14, but from from 20.8 g (0.0784 mol) of of 2-oxo-2-thien-2-ylacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl ester and cyclopentylmagnesium cloride, 0.08 mol (40 ml of a solution 2M in ether). The oil obtained (15.64 g) was purified by chromatography on silica gel eluting with chloroform/methanol/ammonia 97:3:0.5 to obtain 8.38 g (32%) of a pure product, mixture of diastereomers: I-15a and I-15b. Structure confirmed by 1H-NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122558B2
Source datasetuspto-grants-2006_10
ORD IDord-883c30eaedac4e3ba06bf503e3b7a49d
Source noteuspto-grants-2006_10