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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468140Generated: October 30, 2026

Sodium Carbonate → {1-[1-(Diphenylmethyl)azetidin-3-yl]-4-(phenylcarbonyl)piperazin-2-yl}methanol

https://huagongshe.com/reaction/468140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant{1-[1-(Diphenylmethyl)azetidin-3-yl]-piperazin-2-yl}methanolHCID 59625873—
SolventDichloromethaneHCID 6344—
Product{1-[1-(Diphenylmethyl)azetidin-3-yl]-4-(phenylcarbonyl)piperazin-2-yl}methanolHCID 59625708—

Reaction Conditions

Temperature0 °C

Reaction Steps

Compound 37c (1.03 mmol) was dissolved in CH2Cl2 (5 mL) and cooled in an ice water bath to 0° C. A 10% aqueous Na2CO3 solution (5 mL) was added and a solution of compound 37d (143 pt, 1.23 mmol) dissolved in CH2Cl2 (1 mL) was added dropwise. The resultant mixture was allowed to warm to 20° C. and then stirred rapidly for 62 h. CH2Cl2 (10 mL) was added to the reaction mixture and the aqueous phase was extracted with CH2Cl2 (2×20 mL). The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated to give compound 37e (465 mg) as an off white foam. Compound 37e was used in the following step without further purification. 1H NMR (400 MHz, CDCl3): δ 7.39 (m, 9H), 7.22-7.32 (m, 4H), 7.14-7.23 (m, 2H), 4.35 (s, 1H), 4.07 (br. s, 1H), 3.30-3.71 (complex, 8H), 2.2-3.0 (complex, 6H); LCMS m/z (M+H+) 442.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623858B2
Source datasetuspto-grants-2014_01
ORD IDord-6e754a6e84024293876061c041afae2c
Source noteuspto-grants-2014_01