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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409233Generated: October 30, 2026

(S)-(-)-3-Acetamidopyrrolidine → HCID 44251167, compound

https://huagongshe.com/reaction/1409233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(-)-3-AcetamidopyrrolidineHCID 7021471—
ReactantN-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamideHCID 86652267—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 44251167HCID 44251167108.5%

Reaction Steps

In a 2 mL microwave vial were placed N-(7-chloropyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2D, 80 mg, 0.24 mmol) and (S)—N-(pyrrolidin-3-yl)acetamide (62 mg, 0.48 mmol). To the sealed vial were then added NMP (2 ml), and the mixture was then heated in the microwave at 100° C. for 15 minutes. After cooling to room temperature, the reaction mixture was filtered by syringe filter and was then directly purified by preparatory HPLC (20-40% MeCN/H2O gradient+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a white powder (110 mg, 99% yield). 1H NMR (400 MHz, DMSO-d6) δ=10.88 (s, 1H), 8.24 (d, J=6.3 Hz, 1H), 8.02 (d, J=2.3 Hz, 1H), 8.01-7.96 (m, 2H), 7.65-7.59 (m, 2H), 6.87 (s, 1H), 6.29 (d, J=2.0 Hz, 1H), 4.41-4.31 (m, 2H), 2.25-2.13 (m, 1H), 2.03-1.91 (m, 1H), 1.83 (s, 3H), 1.46 (s, 6H); ESI-MS: m/z 423.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921358B2
Source datasetuspto-grants-2014_12
ORD IDord-4a8ce12790df4e2293bd8ee4d7d43e6b
Source noteuspto-grants-2014_12