HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427164Generated: November 2, 2026
Diisopropylethylamine → 9-{[4-(Ethyloxy)phenyl]sulfonyl}-2-methyl-8,9,10,10a-tetrahydropyrido[2',3':3,4]pyrrolo[1,2-a]pyrazin-5(7H)-one
https://huagongshe.com/reaction/1427164
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Ethoxybenzene-1-sulfonyl chloride | HCID 3688334 | — |
| Reactant | 2-Methyl-8,9,10,10a-tetrahydropyrido[2',3':3,4]pyrrolo[1,2-a]pyrazin-5(7H)-one | HCID 70557512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 9-{[4-(Ethyloxy)phenyl]sulfonyl}-2-methyl-8,9,10,10a-tetrahydropyrido[2',3':3,4]pyrrolo[1,2-a]pyrazin-5(7H)-one | HCID 57524289 | 62.9% |
Reaction Steps
To a suspension of 2-methyl-8,9,10,10a-tetrahydropyrido[2′,3′:3,4]pyrrolo[1,2-a]pyrazin-5(7H)-one (may be prepared as described in Intermediate 8; 70 mg) in DCM (5 mL) was added DIPEA (0.241 mL, 1.378 mmol). To this was added 4-(ethyloxy)benzenesulfonyl chloride (80 mg) and this was allowed to stir at room temperature for 30 minutes. The reaction mixture was partitioned between DCM and saturated sodium bicarbonate solution in a hydrophobic frit. The aqueous layer was re-extracted with DCM. The combined organic phases were evaporated to an orange oil. The residue was purified by chromatography (25S silica cartridge) eluting with 0-5% methanol in DCM over 12 column volumes. The clean fractions were combined and evaporated to give the title compound as a white foam (84 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933132B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-bbf8b54f7e754a159771e67e804cd99a |
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| Source note | uspto-grants-2015_01 |
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