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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863Generated: October 23, 2026

Triethylamine → [1-(N-phenylmethoxycarbonylcarbamimidoyl)pyrrolidin-3-yl]methyl methanesulfonate

https://huagongshe.com/en/reaction/863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactantbenzyl N-[3-(hydroxymethyl)pyrrolidine-1-carboximidoyl]carbamateHCID 140379085—
SolventDiethyl EtherHCID 3283—
SolventEthylacetate heptaneHCID 21899848—
Product[1-(N-phenylmethoxycarbonylcarbamimidoyl)pyrrolidin-3-yl]methyl methanesulfonateHCID 14037908750%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.7 g (2.53 mmole) (3RS)-1-(N-benzyloxycarbonylamidino)-3-hydroxymethyl pyrrolidine and 0.70 ml (5.05 mmole) triethylamine was dissolved in 15 ml diethyl ether/CH2Cl2 1/1 and the mixture was cooled to 0° C. 0.25 ml (3.29 mmole) methanesulphonyl chloride in 3 ml diethyl ether was slowly added and the reaction mixture was stirred at 0° C for three hours. The solvent was evaporated and the residue was dissolved in ethyl acetate and extracted with a 0.3M KHSO4 -solution. The water layer was washed once with CH2Cl2. The water layer was made neutral with 10M NaOH-solution and extracted twice with CH2Cl2. The combined organic layer was dried (Na2 SO4), filtered and evaporated to yield 0.450 g (50%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723444
Source datasetuspto-grants-1998_03
ORD IDord-50d2591cf07947e7ab725904f4df96f4
Source noteuspto-grants-1998_03