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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057737Generated: November 2, 2026

1,2-Dichloroethane → HCID 10182672, compound

https://huagongshe.com/reaction/1057737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantGlyceraldehydeHCID 751—
ReactantBMS 387032HCID 3025986—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventMethanolHCID 887—
ProductHCID 10182672HCID 1018267289.3%

Reaction Steps

N-[5-[[[5-(1,1-Dimethylethyl)-2-oxazolyl]methyl]thio]-2-thiazolyl]-4-piperidinecarboxamide (66 mg, 0.17 mmol, 1 eq) was combined with glyceraldehyde (69 mg, 0.77 mmol, 4.5 eq), sodium triacetoxyborohydride (163 mg, 0.77 mmol, 4.5 eq) and 1,2-dichloroethane (4 mL). The resulting suspension was stirred at rt for 4 h. Methanol (1 mL) was added and the reaction mixture was stirred at rt overnight, concentrated in vacuo and purified by preparative HPLC to provide 69 mg (59%) of (±)-1-(2,3-dihydroxypropyl)-N-[5-[[[5-(1,1-dimethylethyl)-2-oxazolyl]methyl]thio]-2-thiazolyl]-4-piperidinecarboxamide as a white solid. MS: 455 [M+H]+; HPLC: 100% at 3.06 min (YMC S5 ODS column 4.6×50 mm, 10-90% aqueous methanol over 4 minutes containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515004B1
Source datasetuspto-grants-2003_02
ORD IDord-d540c7a820144d3a850f8ca0420c6d89
Source noteuspto-grants-2003_02