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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256335Generated: October 31, 2026

Thiomorpholine → HCID 67064040, compound

https://huagongshe.com/reaction/1256335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiomorpholineHCID 67164—
ReactantN-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamideHCID 86652267—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 67064040HCID 6706404039%

Reaction Steps

A solution of N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2F, 99 mg, 0.287 mmol) and thiomorpholine (91 mg, 0.861 mmol) in DMF (1.11 mL) was stirred at 100° C. for 2 h. After cooling to room temperature, the mixture was diluted with methanol and then purified by preparatory HPLC (35-60% MeCN/H2O gradient+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a white solid (26.9 mg, 39%). Melting point (229.1-229.2° C.). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.45 (s, 6 H), 2.38 (s, 3 H), 2.75-2.90 (m, 4 H), 4.02 (dt, J=4.67, 2.46 Hz, 4 H), 6.16 (s, 1 H), 7.35 (s, 1 H), 7.60 (d, J=8.34 Hz, 2 H), 7.99 (d, J=8.34 Hz, 2 H), 10.86 (s, 1 H); ESI-MS: m/z 412.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461163B2
Source datasetuspto-grants-2013_06
ORD IDord-bfbc6a26895942b4ade26982115bbceb
Source noteuspto-grants-2013_06