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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452710Generated: October 31, 2026

Water → HCID 25208190, compound

https://huagongshe.com/reaction/1452710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl chloroformateHCID 6586—
Reactant4-MethylmorpholineHCID 7972—
ReactantHCID 24815128HCID 24815128—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductHCID 25208190HCID 25208190—

Reaction Conditions

Temperature-12 °C

Reaction Steps

50 ml of 2-methyltetrahydrofuran are distilled off from the solution consisting of 9.15 g (28.29 mmol, 1.0 eq) 2-amino-N-[1-(phenylmethyl)-4-piperidinyl]-phenylacetamide in 162 ml of 2-methyltetrahydrofuran. The solution is cooled to −12° C. and 4.56 g (45.10 mmol, 1.6 eq) 4-methylmorpholine are added, followed by 4.26 g (45.10 mmol, 1.6 eq) methyl chloroformate. The reaction mixture is stirred for another 1 hour at 20° C. and then combined with 100 ml of water. After phase separation the aqueous phase is washed with 20 ml 2-methyltetrahydrofuran and the combined organic phases are washed with 50 ml of water. The organic solvent is distilled off in vacuo. The residue is combined with 50 ml of acetone and refluxed. Then 100 ml of water are added and the suspension obtained is cooled to 20° C. To complete the crystallisation the mixture is stirred for 30 minutes at 20° C. Then the product is suction filtered, washed with 30 ml acetone-water mixture (1:2) and dried in the dryer at 45° C. while being rendered inert.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473778B2
Source datasetuspto-grants-2009_01
ORD IDord-82a631e46acf4b84a5cc3c5d45a0e555
Source noteuspto-grants-2009_01