HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416519Generated: October 31, 2026
Propyl isocyanate → HCID 59759894, compound
https://huagongshe.com/reaction/416519
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propyl isocyanate | HCID 61033 | — |
| Reactant | 5-Chloro-Thiophene-2-Carboxylic Acid [2-(1--Isopropyl-Piperidin-4-Ylsulfamoyl)-Ethyl]-Amide | HCID 11990478 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59759894 | HCID 59759894 | — |
Reaction Steps
To a solution of 200 mg (0.50 mmol) 5-chloro-thiophene-2-carboxylic acid [2-(1-isopropyl-piperidin-4-ylsulfamoyl)-ethyl]-amide in 3 ml dichloromethane were added 0.1 ml (2 equiv.) 1-isocyanato-propane and 6 mg DMAP. The reaction mixture was stirred overnight at room temperature. The next day further 0.1 ml (2 equiv.) 1-isocyanato-propane and 6 mg DMAP were added. After stirring for 48 h at room temperature, the reaction mixture was washed with 3 ml water and concentrated under reduced pressure. Final purification by preparative RP-HPLC (CH3CN/H2O gradient+0.1% TFA) gave pure 5-chloro-thiophene-2-carboxylic acid {2-[(1-isopropyl-piperidin-4-yl)-propylaminocarbonyl-sulfamoyl]-ethyl}-amide. The title compound was obtained as its trifluoroacetate in form of a colorless amorphous material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088925B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-89aa969c664548b48ef08c5d5201a76d |
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| Source note | uspto-grants-2012_01 |
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