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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45801Generated: October 29, 2026

Pyrrolidine → tert-butyl 4-[3-carbamoyl-8-(pyrrolidin-1-yl)-1H-pyrazolo[4,3-h]quinazolin-1-yl]piperidine-1-carboxylate

https://huagongshe.com/reaction/45801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactanttert-butyl 4-[3-carbamoyl-8-(methylsulfonyl)-1H-pyrazolo[4,3-h]quinazolin-1-yl]piperidine-1-carboxylateHCID 67975337—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 4-[3-carbamoyl-8-(pyrrolidin-1-yl)-1H-pyrazolo[4,3-h]quinazolin-1-yl]piperidine-1-carboxylateHCID 6797545351.1%

Reaction Steps

To a solution of tert-butyl 4-[3-carbamoyl-8-(methylsulfonyl)-1H-pyrazolo[4,3-h]quinazolin-1-yl]piperidine-1-carboxylate 30 mg (0.063 mmol) in THF (3 ml), pyrrolidine 70 μl (1 mmol) was added. The solution was stirred at room temperature for 1 hour and monitored by LC/MS. The reaction mixture was cooled to room temperature; the separated solid was filtered and washed with diethyl ether to afford tert-butyl 4-[3-carbamoyl-8-(pyrrolidin-1-yl)-1H-pyrazolo[4,3-h]quinazolin-1-yl]piperidine-1-carboxylate 15 mg (50%). LC/MS (m/z): 475.0 [M+H]+, HPLC (254 nm) method 4 Rt 2.01 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541576B2
Source datasetuspto-grants-2013_09
ORD IDord-2036c8af6728491eb9d4a10fac43048d
Source noteuspto-grants-2013_09