HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929721Generated: October 30, 2026
Lawesson's reagent → HCID 22643457, compound
https://huagongshe.com/reaction/929721
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 23512941 | HCID 23512941 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22643457 | HCID 22643457 | 97% |
Reaction Steps
A mixture of N-((4-Methylphenyl)methyl)-N-(1-(phenylmethyl)piperidin-4-yl)-(4-methoxyphenylmethyl)acetamide (20 mg, 0.045 mmol) and Lawesson's reagent (25 mg, 0.062 mmol), was taken in a glass vial and mixed thoroughly with magnetic stirbars. The glass vial was then irradiated in a microwave oven (900 W, Whirlpool M401) for 8 min. Upon completion of the reaction, the yellow-colored material was transferred to an ion-exchange column with the aid of methanol (2 ml). The ion-exchange column was subsequently washed with CH2Cl2 (2 ml) and methanol (2 ml) and the product was thereafter eluted from the ion-exchange column (10% NH3 in methanol, 2 ml) to give N-((4-Methylphenyl)methyl)-N-(1-(phenylmethyl)piperidin-4-yl)-4-methoxyphenylmethyl thioacetamide (20 mg, 97%) as a white solid; LC-MS: (M+H)+ 459, tr 9.60 min; TLC (CH2Cl2/methanol 20:1) Rf=0.38.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296694B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-e380751bcf984b47bf04ea8d4eef0439 |
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| Source note | uspto-grants-2016_03 |
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