HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 12001808, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Hydroxypiperidine, (R)- | HCID 2759334 | — |
| Reactant | 4-Chloro-6-iodo-3-methanesulfonyl-2-methyl-quinoline | HCID 12001624 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12001808 | HCID 12001808 | 60% |
Reaction Steps
4-Chloro-6-iodo-3-methanesulfonyl-2-methyl-quinoline (compound of example D.2) (300 mg, 0.786 mmol), (R)-(+)-3-hydroxypiperidine (119 mg, 0.865 mmol) and N,N-diisopropyl ethyl amine (0.148 mL, 0.865 mmol) were heated in dry N,N-dimethylformamide (3 mL) for 0.5 h at 100° C. N,N-Dimethylformamide was evaporated at 40° C./0.1 mbar, the residue was extracted with dichloromethane and 10% Na2CO3, and then purified by chromatography on silica gel in dichloromethane/methanol 20:1. One obtained a yellow oil which was triturated with ethyl acetate and the resulting white crystals were filtered off. One obtained 209 mg (60%) of white crystals. MS: m/z=447 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728142B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-600ea43f320240e58a7342bd9fbc75b3 |
| Source note | uspto-grants-2010_06 |