Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591354Generated: November 3, 2026

Methylamine → HCID 72725462, compound

https://huagongshe.com/reaction/591354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 89612782HCID 89612782—
SolventMethanolHCID 887—
ProductHCID 72725462HCID 72725462—

Reaction Conditions

Temperature39 °C

Reaction Steps

In a flask was placed methyl 2-(4-(6-fluoroindolin-1-yl)piperidine-1-carboxamido)thiazole-5-carboxylate (80.8 mg, 0.2 mmol) and MeOH (4 mL) was added. Then, 40 wt % CH3NH2(aq) (6 mL) was added and the resulting mixture was heated to 38-40° C. for 4 h. The resulting mixture was concentrated to remove MeOH and then partitioned in CH2Cl2/H2O (30 mL/30 mL). The aqueous layer was extracted with CH2Cl2 (30 mL). The combined organic layer was dried (Na2SO4) and filtered. The solvent was removed by roto-evaporator and the resulting residue re-solidified from CH2Cl2/hexane to yield 2-(4-(6-fluoroindolin-1-yl)piperidine-1-carboxamido)-N-methylthiazole-5-carboxamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238658B2
Source datasetuspto-grants-2016_01
ORD IDord-e53979b1d99948b7a6fe7f216c376e7e
Source noteuspto-grants-2016_01