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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382122Generated: November 1, 2026

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → 4-Methyl-2-thiazol-2-yl-pyrimidine-5-carboxylic acid (3-ethyl-5-fluoro-pyrrolo[2,3-b]pyridin-1-yl)-amide

https://huagongshe.com/reaction/2382122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
Reactant4-methyl-2-(2-thiazolyl)-5-Pyrimidinecarboxylic acidHCID 68553630—
ReactantHCID 68555593HCID 68555593—
SolventDimethylformamideHCID 6228—
SolventSodium CarbonateHCID 10340—
Product4-Methyl-2-thiazol-2-yl-pyrimidine-5-carboxylic acid (3-ethyl-5-fluoro-pyrrolo[2,3-b]pyridin-1-yl)-amideHCID 5919997466.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of 4-methyl-2-thiazol-2-yl-pyrimidine-5-carboxylic acid (509 mg, 2.28 mmol) and 3-ethyl-5-fluoropyrrolo[2,3-b]pyridin-1-ylamine (340 mg, 1.9 mmol) in DMF (6 mL) is stirred at 40° C. for 1 h. The mixture is treated with DMTMM (524 mg, 1.9 mmol) and stirred at 40° C. for 1 h. The mixture is diluted with saturated aqueous Na2CO3 (5 mL) and stirred for 5 min. The precipitate is collected by filtration and dried in vacuo to afford 4-methyl-2-thiazol-2-yl-pyrimidine-5-carboxylic acid (3-ethyl-5-fluoro-pyrrolo[2,3-b]pyridin-1-yl)-amide (481 mg, 66%). MS: 383 (M+H); 1H NMR (300 MHz, DMSO-d6): δ 11.95 (s, NH, 1H), 9.10 (s, 1H), 8.29 (s, 1H), 8.14 (d, 1H), 8.08 (d, 1H), 8.00 (m, 1H), 7.57 (s, 1H), 2.79 (s, 3H), 2.75 (q, 2H), 1.29 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-520df424142d49699577d2c802236e87
Source noteuspto-grants-2012_09