HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966224Generated: October 31, 2026
Chloroacetaldehyde → HCID 25261177, compound
https://huagongshe.com/reaction/1966224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | HCID 86644603 | HCID 86644603 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 25261177 | HCID 25261177 | 47% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420642B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-fc46fee2bab34a6f9e21fcd534eacf75 |
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| Source note | uspto-grants-2013_04 |
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