HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044715Generated: October 31, 2026
Hydrochloric Acid → HCID 178464667, compound
https://huagongshe.com/reaction/1044715
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amine | HCID 3513851 | — |
| Reactant | 3-Bromo-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride | HCID 58158706 | — |
| Reactant | HCID 178464603 | HCID 178464603 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178464667 | HCID 178464667 | 78.4% |
Reaction Steps
To a solution of 1.20 g N-ethyl-4,4-dimethyl-4,5-dihydro-pyrazole-1-carboxamidine hydrochloride in 35 mL dry THF was added 5.1 mL (3.0 equiv.) BEMP and the reaction mixture was stirred for 10 minutes at room temperature. 2.15 g (1.0 equiv.) 3-Bromo-4-(2,2,2-trifluoro-acetylamino)-benzenesulfonyl chloride was added in one portion and the resulting bright yellow solution was stirred overnight at room temperature. The reaction mixture was acidified with 1N HCl and extracted twice with EA. The combined organic layers were dried over Na2SO4, filtered and evaporated under reduced pressure. Purification by flash chromatography (Et2O/PA 1:1→Et2O) afforded 2.29 g (78%) of product. 1H NMR (400 MHz, CDCl3) δ 1.18 (t, J=7.3 Hz, 3H), 1.24 (s, 6H), 3.43-3.51 (m, 2H), 3.79 (br.s, 2H), 6.78 (s, 1H), 7.93 (dd, J=8.6, 2.0 Hz, 1H), 8.19 (d, J=2.0 Hz, 1H), 8.39 (d, J=8.6 Hz, 1H), 8.61 (br.s., 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563723B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-6502296579454a179c9a8d521ec61f53 |
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| Source note | uspto-grants-2013_10 |
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