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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048228Generated: November 2, 2026

Methyl N-(triethylammoniosulfonyl)carbamate → HCID 68000904, compound

https://huagongshe.com/reaction/1048228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
ReactantHCID 68000416HCID 68000416—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 68000904HCID 68000904—

Reaction Steps

A solution of 58 mg (0.115 mmol) of (S)—N′-acetyl-2-((3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-2-oxopiperidin-1-yl)butanehydrazide (Example 34, Step A) and Burgess' reagent (110 mg, 0.462 mmol) in dichloroethane (1154 μL) was heated in the microwave at 120° C. for 30 min. Then the reaction mixture was diluted with water and extracted with DCM. The combined organic layers were washed with sat. aq. NaCl and NaHCO3-solutions, dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. Separation by reversed phase HPLC (55 to 90% MeCN/H2O in 35 min, 29 mg injection each time) provided the title compound as a colorless film. MS (ESI) 484.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-a53e0077573b4640b20cd5401d282087
Source noteuspto-grants-2013_10