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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242791Generated: October 30, 2026

Phenylacetyl chloride → HCID 21939585, compound

https://huagongshe.com/reaction/1242791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDichloromethaneHCID 6344—
ProductHCID 21939585HCID 21939585100%

Reaction Steps

BOC-Piperazine (1.06 g) was combined with dichloromethane (20.0 mL) and diisopropylethylamine (1.49 mL). Phenylacetylchloride (0.90 mL) was added dropwise and the reaction was allowed to stir at room temperature for 24 hours. The reaction was then washed with HCl (1N in water, 3×5 mL), saturated aqueous sodium bicarbonate (3×5 mL) and brine (5 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated giving 1-BOC-4-phenylacetamidopiperazine (1.73 g). Yield=100% Step 2: The BOC group was removed from 1-BOC-4-phenylacetamidopiperazine according to example 137 giving phenylacetamidopiperazine hydrochloride. Yield=93%. Step 3: Phenylacetamidopiperazine hydrochloride was reacted with 8-ethyl-6-chloropurine (Example 140) according to Example 87. Yield=27%, ES-MS: (M+H)+ 351.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115741B2
Source datasetuspto-grants-2006_10
ORD IDord-cb6d587a2c7d4577a0f3b334d7929e8c
Source noteuspto-grants-2006_10