HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427310Generated: October 28, 2026
4-Methylmorpholine → HCID 70562192, compound
https://huagongshe.com/reaction/1427310
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | HCID 70565237 | HCID 70565237 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70562192 | HCID 70562192 | — |
Reaction Steps
Ethanesulfonyl chloride (0.26 g, 2 mmol) was added to a stirred solution of methyl 2-(4-amino-1H-indol-1-yl)-2-(4-chlorophenyl)butanoate (0.58 g, 1.7 mmol), as described in Example 3 Step B, and 4-methylmorpholine (0.25 g, 2.5 mmol) in DCM (8 mL) at 0° C. After 30 min, an additional portion of ethanesulfonyl chloride (0.1 g, 1 mmol) was added. After 1 h, the reaction mixture was partitioned between DCM and saturated aqueous ammonium chloride. The layers were separated and the aqueous layer was extracted with DCM. The combined organic layers were washed with brine, dried sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel flash chromatography (PE:EA=2:1) to afford the title compound. LC/MS m/z=435.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933113B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-3ead65c0c8df4bd09e165ce8fd9f97a9 |
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| Source note | uspto-grants-2015_01 |
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