HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Trifluoromethylbenzenesulphonyl chloride → 1-(2-Trifluoromethyl-benzenesulfonyl)-1,6-diaza-spiro[3.3]heptane-6-carboxylic acid (3-phenyl-propyl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Trifluoromethylbenzenesulphonyl chloride | HCID 136616 | — |
| Reactant | 6-(3-Phenyl-propylcarbamoyl)-1,6-diaza-spiro[3.3]heptane-1-carboxylic acid tert-butyl ester | HCID 86682351 | — |
| Product | 1-(2-Trifluoromethyl-benzenesulfonyl)-1,6-diaza-spiro[3.3]heptane-6-carboxylic acid (3-phenyl-propyl)-amide | HCID 71555050 | — |
Reaction Steps
In analogy to the experimental procedure of example 6b) 6-(3-phenyl-propylcarbamoyl)-1,6-diaza-spiro[3.3]heptane-1-carboxylic acid tert-butyl ester instead of tert-butyl 1-(2,4-dichlorobenzylcarbamoyl)-1,6-diazaspiro[3.3]heptane-6-carboxylate was converted using 2-trifluoromethylbenzene-1-sulfonyl chloride instead of 4-chlorobenzene-1-sulfonyl chloride into the title compound which was obtained as an off-white solid (38 mg, 25%). MS m/e: 468 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809552B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-1b32083a13db46008c63431a2ed6cdf6 |
| Source note | uspto-grants-2014_08 |