HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773616Generated: November 2, 2026
1,2-Diaminocyclohexane, cis- → HCID 56646341, compound
https://huagongshe.com/reaction/1773616
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Diaminocyclohexane, cis- | HCID 342917 | — |
| Reactant | HCID 66664866 | HCID 66664866 | — |
| Reactant | HCID 86661376 | HCID 86661376 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 56646341 | HCID 56646341 | — |
Reaction Steps
A suspension of the mixture of 80 mg of 2-Chloro-thieno[3,2-d]pyrimidine-7-carboxylic acid benzo[1,3]dioxol-5-ylamide and 2-(Benzotriazol-1-yloxy)-thieno[3,2-d]pyrimidine-7-carboxylic acid benzo[1,3]dioxol-5-ylamide (from step a) and 0.17 g (1.41 mmole) of cis-1,2-diaminocyclohexane in Dioxane (3 mL) was stirred at 60° C. for overnight. The reaction were cooled down and diluted with CH2Cl2, washed with aqueous Na2CO3, brine, dried over anhydrous Na2SO4, concentrated and purified by flash chromatography (silica gel, 40 g, 0% to 30% MeOH (0.7 N) in CH2Cl2) to 40 mg of 2-(cis-2-Amino-cyclohexylamino)-thieno[3,2-d]pyrimidine-7-carboxylic acid benzo[1,3]dioxol-5-ylamide as light yellow solid. MH+/Z=412.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255110B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-fbb3b9215f804c0f8d51aec260dc161b |
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| Source note | uspto-grants-2016_02 |
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