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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045950Generated: October 29, 2026

(Methylthio)acetic acid → HCID 54766757, compound

https://huagongshe.com/reaction/2045950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Methylthio)acetic acidHCID 75551—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
ReactantHCID 66587222HCID 66587222—
SolventDichloromethaneHCID 6344—
ProductHCID 54766757HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592418B2
Source datasetuspto-grants-2013_11
ORD IDord-ef0da886472b43a4a84c0e8bccdf10cc
Source noteuspto-grants-2013_11