HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphosgene → N-tetrahydrofurfuryl-5-methyl-3-(3-trifluoromethylphenyloxy)pyrazole-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | Tetrahydrofurfurylamine | HCID 253298 | — |
| Reactant | 5-Methyl-3-(3-trifluoromethylphenyloxy)pyrazole | HCID 17862420 | — |
| Product | N-tetrahydrofurfuryl-5-methyl-3-(3-trifluoromethylphenyloxy)pyrazole-1-carboxamide | HCID 67066650 | 70.3% |
Reaction Steps
5-Methyl-3-(3-trifluoromethylphenyloxy)pyrazole reacted with trichloromethyl chloroformate in the same manner as in Example 198 and then reacted with tetrahydrofurfurylamine to give a white solid of N-tetrahydrofurfuryl-5-methyl-3-(3-trifluoromethylphenyloxy)pyrazole-1-carboxamide (yield: 70.3%). mp: 101-102° C.; 1H-NMR (CDCl3, TMS, ppm): δ 1.56-1.67 (m, 1H), 1.84-2.05 (m, 3H), 2.60 (s, 3H), 3.29-3.39 (m, 1H), 3.55 (ddd, J=3.8, 6.1 and 13.8 Hz, 1H), 3.70-3.90 (m, 2H), 4.00-4.10 (m, 1H), 5.74 (s, 1H), 7.21 (br s, 1H), 7.33-7.37 (m, 1H), 7.40-7.51 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700786B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-43ec7c3ecc8547d380026a6091bed480 |
| Source note | uspto-grants-2010_04 |