HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910667Generated: October 28, 2026
Diisopropylethylamine → 4-(4-Thiophen-3-yl-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/910667
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(4-Chloro-6-thiophen-3-yl-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 86628634 | — |
| Solvent | Isopropanol ethyl acetate | HCID 22055037 | — |
| Product | 4-(4-Thiophen-3-yl-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 67387808 | — |
Reaction Steps
To a solution of 4-(4-chloro-6-thiophen-3-yl-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester (169 mg, 0.29 mmol) in 2-propanol/EtOAc (10:1, 11 mL) at room temperature was added DIEA (0.5 mL). The resulting solution was vacuum-flushed with N2 and then treated with 10% Pd/C (50 mg). The resulting suspension was exposed to H2 via balloon and heated to 65° C. After 3 h, 10% Pd/C (50 mg) was added, and the reaction mixture was heated at 65° C. overnight under H2. The resulting mixture was filtered to remove catalyst; the filtrate was concentrated and the residue was purified by preparative TLC (EtOAc/hexanes, 1:2) to yield a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022209B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-73fb8145f6714d46ad4b034a9a9605cc |
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| Source note | uspto-grants-2011_09 |
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