HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733665Generated: October 30, 2026
Methanesulfonic Acid → HCID 68867276, compound
https://huagongshe.com/reaction/733665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | HCID 57840771 | HCID 57840771 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68867276 | HCID 68867276 | — |
Reaction Steps
A mixture of 7-chloro-3-methyl-4-(1-morpholin-4-yl-methanoyl)-pyrrolo[2,3-c]pyridine-1-carboxylic acid tert-butyl ester, 3-bromoaniline (56 μl), and methanesulfonic acid (33 μl) in 1,4-dioxane (2 ml) was heated under microwave conditions at 180° C. for 30 minutes. The solid mass obtained was dissolved in methanol, transferred to a round bottom flask and evaporated. The residue was dissolved in ethyl acetate and washed with 5% sodium hydrogen carbonate solution and water. The organic layer was dried (MgSO4) and evaporated to give an off-white solid. The solid was triturated with diethyl ether, filtered off and sucked dry. The solid was then dissolved in warm ethyl acetate (10 ml) and treated with a solution of 1M hydrochloric acid in diethyl ether (10 drops). The resultant solid precipitate was then filtered off, sucked dry then dried at 40° C. under vacuum to afford the title compound (58 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589206B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-8128d167f3f04bfa92f9097847838a21 |
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| Source note | uspto-grants-2009_09 |
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