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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920217Generated: November 1, 2026

Triethylamine → HCID 59226411, compound

https://huagongshe.com/reaction/1920217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 59226409HCID 59226409—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 59226411HCID 5922641185%

Reaction Steps

To a solution of tert-butyl 6-hydroxy-3-(3-nitropyridin-4-yl)cyclohex-2-enylcarbamate (1.0 equiv.) and triethyl amine (1.5 equiv.) in CH2Cl2 (0.2 M) was added methanesulfonyl chloride (1.2 equiv.) at 0° C. The mixture was stirred for 2 hours at that temperature. The reaction mixture was diluted with ethyl acetate, and washed with sat NaCl. The organic was dried with MgSO4, filtered and concentrated to give 2-(tert-butoxycarbonylamino)-4-(3-nitropyridin-4-yl)cyclohex-3-enyl methanesulfonate (85%), which was used in the next step without further purification. LC/MS (m/z): MH+=414.0, Rt=0.82

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168794B2
Source datasetuspto-grants-2012_05
ORD IDord-3c349ec2954444d7be8b15b2a118a4ff
Source noteuspto-grants-2012_05