HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745845Generated: October 30, 2026
Iodo benzene diacetate → HCID 129849852, compound
https://huagongshe.com/reaction/1745845
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | HCID 178518853 | HCID 178518853 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 129849852 | HCID 129849852 | — |
Reaction Steps
With reference to EXAMPLE 1-1, 5 mg (0.016 mmol) of iodobenzene diacetate was added to a mixture of 5 mg (0.017 mmol) of 4-(ferrocenylmethyl)urazole and 0.25 mL of tetrahydrofuran at room temperature. The mixture was stirred for 2 hours to give the tetrahydrofuran solution of 4-(ferrocenylmethyl)-1,2,4-triazoline-3,5-dione. A tetrahydrofuran (0.25 mL) solution of 1 mg (0.0025 mmol) of alfacalcidol prepared in accordance with the method described in Japanese Patent Publication (KOKAI) No. 48-62750, Tetrahedron Lett., 1973, 2339 and Tetrahedron, 30, 2701 (1974) was added to the resulting solution, followed by stirring at room temperature for an hour. The resulting mixture was concentrated under reduced pressure and the residue obtained was purified by thin layer silica gel chromatography (hexane:ethyl acetate=1:2) to give 1 mg (57%) of the titled alfacalcidol/4-(ferrocenylmethyl)-1,2,4-triazoline-3,5-dione adduct (ALF-FMTAD) as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07019146B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-bb43aef7b4f04809a48615bc3938042c |
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| Source note | uspto-grants-2006_03 |
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