Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966224Generated: October 31, 2026

Chloroacetaldehyde → HCID 25261177, compound

https://huagongshe.com/reaction/1966224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantHCID 86644603HCID 86644603—
SolventDimethylformamideHCID 6228—
ProductHCID 25261177HCID 2526117747%

Reaction Conditions

Temperature100 °C

Reaction Steps

(3-Cyclopentyloxy-5-phenoxy-pyridine-2-yl)-thiourea (0.29 mmol) is dissolved in DMF (1 ml) and chloro-acetaldehyde (1.1 eq., 55% in water) is added and stirred 3 h at 100° C. After cooling to room temperature the suspension is pored into ice-water and extracted with methyl-ter.-butyl ether. The combined organic phases are washed with brine and dried over MgSO4. The solvent is removed in vacuo. (3-Cyclopentyloxy-5-phenoxy-pyridine-2-yl)-thiazole-2-yl-amine (“A21”) is obtained after reversed phase chromatography (water/acetonitrile+0.1% TFA) as yellow solid in a yield of 47%; 138.2-139.7°; HPLC (method C): 2.00 min; LC-MS (method A): 2.00 min, 354.1 (M+H+);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420642B2
Source datasetuspto-grants-2013_04
ORD IDord-fc46fee2bab34a6f9e21fcd534eacf75
Source noteuspto-grants-2013_04