Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722022Generated: October 31, 2026

Acetylacetone → HCID 178426467, compound

https://huagongshe.com/reaction/722022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetylacetoneHCID 31261—
ReactantHCID 178479354HCID 178479354—
ProductHCID 178426467HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138397B2
Source datasetuspto-grants-2006_11
ORD IDord-db2ccf28acbc4267bc582bbb855ad56e
Source noteuspto-grants-2006_11