HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810986Generated: November 2, 2026
1,2-Dichloroethane → HCID 59548746, compound
https://huagongshe.com/reaction/1810986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-methyl-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridin-2-amine | HCID 2397998 | — |
| Reactant | 2-(4-(Tert-butoxycarbonyl)piperazin-1-yl)benzoic acid | HCID 2756776 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59548746 | HCID 59548746 | 85% |
Reaction Steps
Dissolved 4-(2-carboxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (0.30 g, 0.98 mmol), EDC (0.23 g, 1.20 mmol) and HOBT (0.18 g, 1.20 mmol) into 1 mL of DMF. The mixture stirred for 1 h. To this is added 5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-ylamine (0.16 g, 0.98 mmol) and N,N-diisopropylethylamine (0.37 mL, 2.00 mmol). The mixture is placed under a stream of Ar and heated at 50° C. for 16 h. The mixture is then diluted with 50 mL CH2Cl2, quenched with 20 mL of saturated NH4Cl; washed with 2×20 mL of H2O, and washed with 1×20 mL of brine. The resultant organic phase was dried with MgSO4, filtered and concentrated to provide 0.38 g, 85% yield of 4-[2-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-ylcarbamoyl)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362249B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-450bf91f57f248ad84c22706020db5ed |
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| Source note | uspto-grants-2013_01 |
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