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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359387Generated: October 29, 2026

Dimethylformamide → HCID 15670868, compound

https://huagongshe.com/reaction/359387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant4-(3-Chloro-2-hydroxypropyl)-1-diphenylmethylpiperazineHCID 10360175—
ReactantHCID 178527891HCID 178527891—
ProductHCID 15670868HCID 15670868—

Reaction Steps

Triethylamine (0.7 mL, 5 mmol) and 1-(1-chloro-2-hydroxy3-propanyl)-4-(diphenylmethyl)piperazine (1.72 g, 5 mmol) was added to 4-mercapto-1H-pyrazolo[3,4-d]pyrimidine (0.78g, 5 mmol) in DMF (10 mL) in portions over a 5 min period. The solution was stirred under nitrogen for 4 days and DMF was removed under vacuum (50° C., 0.5 mmHg). The residue was dissolved in methylene chloride and the solution was washed with water (1×100 mL), saturated brine (1×100 mL) and the organic layer was filtered through celite and evaporated to give a foam (1.47 g). The crude material was eluted through silica gel using 10% methanol: methylene chloride which was extracted with methylene chloride and the organic layer was dried over Na2SO4 and evaporated and dried in vacuo to give the title compound, 0.36 g (13.9%), mp 87°-92° C. 400 MHz 1H NMR (CDCl3) δ: 8.70 (s, 1H), 8.1 (s, 1H), 7.4 (m, 5H), 7.15 (m, 5H), 4.25 (s, 1H), 4.11 (m, 1H), 3.55 (m, 2H), 3.7-2.4 (m, 15H). DCI/MS (M+1) 517.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001127
Source datasetuspto-grants-1991_03
ORD IDord-addea6814e97419c98e987b42765dc16
Source noteuspto-grants-1991_03