HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylacetone → HCID 178426467, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | HCID 178479354 | HCID 178479354 | — |
| Product | HCID 178426467 | HCID 178426467 | — |
Reaction Steps
Using trans-4-(benzyloxycarbonylamino)-1-cyclohexanecarboxamidine-hydrochloride (a compound of Reference Example 8-35 (5)) (348 mg) as a starting material, by reacting the same with acetylacetone according to the method of Libman et al. (J. Chem. Soc., p. 2305, 1952), trans-1-benzyloxycarbonylamino-4-(4,6-dimethylpyrimidin-2-yl)cyclohexane (220 mg) was obtained. By treating this compound (205 mg) with trimethylsilyl iodide in the same manner as in Reference Example 8-35 (7), trans-4-(4,6-dimethylpyrimidin-2-yl)cyclohexylamine (Reference Example 8-36 in Table 9) (129 mg) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07332487B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-19dee25a8bb04f119c4d2297ad81c4cb |
| Source note | uspto-grants-2008_02 |