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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929780Generated: November 3, 2026

2,4-Dichloro-1,3,5-triazine → HCID 68442457, compound

https://huagongshe.com/reaction/1929780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-1,3,5-triazineHCID 17810—
ReactantCis tert-Butyl 4-aminocyclohexylcarbamateHCID 2756050—
ReactantHCID 15839928HCID 15839928—
SolventDichloromethaneHCID 6344—
ProductHCID 68442457HCID 68442457—

Reaction Conditions

Temperature0 °C

Reaction Steps

(R)-3-Amino-pyrrolidine-1-carboxylic acid allyl ester (1 eq.) is dissolved in DCM. The reaction mixture is cooled to 0° C. and a solution of 2,4-dichloro-[1,3,5]triazine (1 eq.) in DCM is added dropwise. The reaction mixture is stirred at room temperature for 2 hours. The reaction mixture is re-cooled to 0° C. and a solution of (4-amino-cyclohexyl)-carbamic acid tert-butyl ester (1 eq.) in DCM is added dropwise. The reaction mixture is stirred at room temperature overnight. The reaction mixture is partitioned between (0.2 M) HCl(aq) and DCM. The organics are washed with water, saturated NaHCO3(aq) and brine. The combined organics are dried (MgSO4), filtered and reduced in vacuo, to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188100B2
Source datasetuspto-grants-2012_05
ORD IDord-50883605084c42f4b531ea2a6f41316c
Source noteuspto-grants-2012_05