HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363739Generated: October 28, 2026
Diisopropylethylamine → HCID 86629874, compound
https://huagongshe.com/reaction/1363739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Acetamido-1,3-thiazole-5-sulfonyl chloride | HCID 350261 | — |
| Reactant | HCID 2543180 | HCID 2543180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86629874 | HCID 86629874 | 59% |
Reaction Steps
A mixture of N,N-diethyl-2-methylamino-acetamide (12 mmol), 2-acetylamino-thiazole-5-sulfonyl chloride (12 mmol) (prepared as described in J. Am. Chem. Soc 69, 2063, 1947), DIPEA (15 mmol) in DCM (50 mL) was stirred at room temperature over night. The reaction mixture was diluted with DCM (50 mL) washed with 10% aq NaHSO4, water and brine, dried and concentrated to give 2-[(2-acetylamino-thiazole-5-sulfonyl)-methyl-amino]-N,N-diethyl-acetamide (59%) as pale yellow crystals. This was suspended in EtOH (10 mL) and added 8N HCl in dioxane (10 mL) and heated for 3H at 80° C. and then cooled to room temperature and concentrated in vacuo to give 2-[(2-amino-thiazole-5-sulfonyl)-methyl-amino]-N,N-diethyl-acetamide as a hydrochloride as colourless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884210B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-d86d5a7ef9a847e58cf12010fd035fb2 |
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| Source note | uspto-grants-2011_02 |
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