Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961909Generated: October 30, 2026

Glycine → HCID 57989962, compound

https://huagongshe.com/reaction/1961909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycineHCID 750—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 57989926HCID 57989926—
Solvent1-ButanolHCID 263—
ProductHCID 57989962HCID 5798996225%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of N-{3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]phenyl}-3-fluorobenzenesulfonamide (100 mg, 0.20 mmol) in 1-butanol (5 mL) was added glycine (153 mg, 2.0 mmol) and K2CO3 (566 mg, 4.0 mmol). The reaction was stirred at 60° C. for 16 h, then partitioned between water and EtOAc. The pH of the aqueous layer was adjusted to below 4 with 1 N HCl, and the aqueous layer was extracted with EtOAc. This organic layer was dried over anhydrous Na2SO4, filtered, and concentrated to generate the title compound as a white powder (24 mg, 0.05 mmol, 22.8% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.04 (d, J=4.5 Hz, 1H), 7.46-7.64 (m, 5H), 7.33 (t, J=8.1 Hz, 1H), 7.18-7.24 (m, 3H), 6.07 (s, 1H), 3.89 (s, 2H), 3.25-3.29 (m, 1H), 1.36 (d, J=6.7 Hz, 6H). MS (ESI): 528.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415345B2
Source datasetuspto-grants-2013_04
ORD IDord-847e2637058245428baca4d99015caba
Source noteuspto-grants-2013_04