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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103679Generated: October 30, 2026

Pyrrolidine → HCID 178419316, compound

https://huagongshe.com/reaction/2103679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-(6-Bromobenzothiazol-2-yl)cyclobutanoneHCID 67145925—
SolventMethanolHCID 887—
ProductHCID 178419316HCID 17841931655%

Reaction Steps

Pyrrolidine (295 μl, 3.54 mmol) was added to a solution of the product of Example 1C (100 mg, 0.354 mmole) in 2 ml methanol and the mixture was stirred at room temperature for 1 hour. Sodium cyanoborohydride (56 mg, 0.891 mmole) was added and the resulting mixture was stirred at room temperature overnight. The reaction was quenched with water and extracted three times with dichloromethane. The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated to give the crude product which was purified by column chromatography (0.5% ammonium hydroxide and 5% methanol in dichloromethane) to give 65 mg (55%) of the title compound. 1H NMR (400 MHz, CDCl3) for the cis isomer δ ppm 7.97 (d, J=1.84 Hz, 1H) 7.80 (d, J=8.90 Hz, 1H) 7.54 (dd, J=8.75, 1.99 Hz, 1H) 3.56-3.66 (m, 1H) 3.05-3.19 (m, 1H) 2.55-2.75 (m, 6H) 2.41-2.53 (m, 2H) 1.75-1.92 (m, 4H). MS: (M+H)+=337/339.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576110B2
Source datasetuspto-grants-2009_08
ORD IDord-54c6ef62d32949b1ba54d5d228ee88b0
Source noteuspto-grants-2009_08