HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084939Generated: October 29, 2026
Diisopropylethylamine → HCID 59756970, compound
https://huagongshe.com/reaction/2084939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-But-2-ynyloxy-benzenesulfonyl chloride | HCID 11195928 | — |
| Reactant | HCID 59756971 | HCID 59756971 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59756970 | HCID 59756970 | — |
Reaction Steps
To a stirred solution of ethyl amino{1-benzyl-4-[(2-hydroxyethyl)sulfanyl]-4-piperidinyl)acetate (2.1 g, 5 mmol) and 4-but-2-ynyloxy benzenesulfonyl chloride (1.24 g, 5.1 mmol) in dichloromethane (200 ml) at 0° C., N,N-diisopropylethylamine (3.0 g, 23.6 mmol) was added slowly. After the addition, the reaction mixture was stirred at room temperature for 4 h and quenched with water. The reaction mixture was washed with water, dried over anhydrous MgSO4, filtered and concentrated. It was purified by silica gel column chromatography eluting with 80% ethyl acetate:hexane to give ethyl {1-benzyl-4-[(2-hydroxyethyl)sulfanyl]-4-piperidinyl}({[4-(2-butynyloxy)phenyl]sulfonyl}amino)acetate as a brown oil; Yield: 1.0 g (85%); Electrospray Mass Spec: 561 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06716833B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-570ffcc6d171428eb60b1bc5cb1c22db |
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| Source note | uspto-grants-2004_04 |
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