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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dichloro-1,3,5-triazine | HCID 17810 | — |
| Reactant | Cis tert-Butyl 4-aminocyclohexylcarbamate | HCID 2756050 | — |
| Reactant | HCID 15839928 | HCID 15839928 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68442457 | HCID 68442457 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188100B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-50883605084c42f4b531ea2a6f41316c |
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| Source note | uspto-grants-2012_05 |
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