HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045950Generated: October 29, 2026
(Methylthio)acetic acid → HCID 54766757, compound
https://huagongshe.com/reaction/2045950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Methylthio)acetic acid | HCID 75551 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 66587222 | HCID 66587222 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54766757 | HCID 54766757 | — |
Reaction Steps
(Methylthio)acetic acid (29 μl), PyBOP (126 mg) and Hünig base (115 μl) is added to a solution of C-{5-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-3-methyl-thiophen-2-yl}-methylamine (90 mg) in dichloromethane (2 ml). After 1 hour at room temperature, the reaction is quenched with water. The reaction mixture is extracted three times with dichloromethane. The combined organic phases are extracted with a saturated solution of NaHCO3 and with a saturated aqueous solution of NaCl, dried over Na2SO4 and concentrated in vacuo. The crude product is purified on a semi-preparative HPLC to yield N-{5-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-3-methyl-thiophen-2-ylmethyl}-2-methylsulfanyl-acetamide (82 mg, compound 1.10 in Table 1) as a white foam. MS (HPLC/MS): 497 (MH+). Retention time: 2.00 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592418B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-ef0da886472b43a4a84c0e8bccdf10cc |
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| Source note | uspto-grants-2013_11 |
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