HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 86615499, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Propanesulfonyl chloride | HCID 82408 | — |
| Reactant | HCID 68456169 | HCID 68456169 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86615499 | HCID 86615499 | — |
Reaction Steps
The product from Example 165d (43 mg, 0.085 mmol) was reacted with isopropylsulfonyl chloride (14.5 mg, 0.102 mmol), N,N-diisopropylethylamine (33 mg, 0.255 mmol), and catalytic DMAP in CH2Cl2 for 18 h giving the crude title compound which was purified by HPLC with TFA providing the product as the trifluoroacetic acid (16 mg, 31%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 1.38 (d, J=6.99 Hz, 6H) 2.73 (s, 3H) 3.54-3.65 (m, 1H) 6.69 (d, J=6.99 Hz, 1H) 7.01 (d, J=9.19 Hz, 2H) 7.20 (d, J=9.19 Hz, 2H) 7.27 (d, J=8.82 Hz, 1H) 7.60 (dd, J=8.82, 2.57 Hz, 1H) 7.70-7.75 (m, 2H) 8.51 (d, J=6.99 Hz, 1H) 8.81 (d, J=8.82 Hz, 1H); MS (ESI+) m/z 484 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338605B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-0b389e7593784587b6baf8c8c097bcc4 |
| Source note | uspto-grants-2012_12 |