HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579433Generated: October 30, 2026
Dimethylformamide → HCID 86683409, compound
https://huagongshe.com/reaction/579433
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 67447923 | HCID 67447923 | — |
| Reactant | HCID 86683400 | HCID 86683400 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86683409 | HCID 86683409 | 26% |
Reaction Conditions
| Temperature | 0.11999999731779099 °C |
|---|
Reaction Steps
A mixture of 6-methoxy-1,2,3,4-tetrahydro-isoquinoline-5-carbaldehyde hydrochloride (82 mg, 0.36 mmol), anhydrous dimethylformamide (5 mL), (2-chloro-4-methyl-thiazol-5-yl)-morpholin-4-yl-methanone (89 mg, 0.36 mmol) and freshly dried potassium carbonate (149 mg, 1.08 mmol) was stirred under argon at 0.120° C. for 3.5 h and then at 150° C. for 1 h. Water (20 mL) was added and the separated solid product was filtered off. The filtrate was extracted with diethyl ether (5×10 mL) and the combined extracts were washed with water (2×10 mL), dried and concentrated. The residue and the above solid product were combined and triturated repeatedly with diisopropyl ether. In this manner the title compound (37 mg, 0.092 mmol, 26%) was obtained as a beige powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040714B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-c1eda36c53ce489cb3a4c2fc9b353d87 |
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| Source note | uspto-grants-2015_05 |
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