HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350749Generated: October 30, 2026
Dimethylformamide → HCID 87796335, compound
https://huagongshe.com/reaction/350749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | HCID 86597659 | HCID 86597659 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 87796335 | HCID 87796335 | — |
Reaction Steps
A mixture of 3-[2-amino-4-(4-chlorophenyl)-5-thiazolyl]-N-[4-(diethylphosphonomethyl)phenyl]propionamide (500 mg), N,N-dimethylformamidedimethylacetal (155 mg) and N,N-dimethylformamide (10 ml) was stirred at room temperature for 1 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography and 3-(4-(4-chlorophenyl)-2-{(E)-[(dimethylamino)methylidene]amino}-5-thiazolyl)-N-[4-(diethylphosphonomethyl)phenyl]propionamide was obtained as crystals (510 mg, yield: 92%) from a fraction eluted with 5% methanol-ethyl acetate. Recrystallization from ethyl acetate gave colorless prism crystals. melting point: 150–151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183276B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-26924503f8ee45b49b1b2c65d64de2a2 |
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| Source note | uspto-grants-2007_02 |
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