Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66605083 | HCID 66605083 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66605534 | HCID 66605534 | 91.9% |
Reaction Steps
1.8 g (5 mmol) of methyl 4-[allyl(mesitylacetyl)amino]-1,3-thiazole-5-carboxylate were initially charged in 5 ml of N,N-dimethylformamide and cooled to 0° C. 1.5 eq of sodium hydride (60%) were added and allowed to warm up gradually to room temperature (RT). After stirring at RT for one hour, 5 ml of water were added and the mixture was acidified to pH 1-2. The precipitate formed was filtered off with suction. 1.5 g of inventive compound I-a-2 were thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686000B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-47f8a0f4351144f482232bfad7b6b3cb |
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| Source note | uspto-grants-2014_04 |
|---|