HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 58864153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | 7-Chloro-4-(1-piperazinyl)-2-quinolinamine | HCID 21101748 | — |
| Reactant | HCID 69514883 | HCID 69514883 | — |
| Product | HCID 58864153 | HCID 58864153 | — |
Reaction Steps
As described for example 78, (3R)-1-acetylhexahydro-1H-azepin-3-amine, 4-nitrophenyl chloroformate, diisopropyl(ethyl)amine, and 7-chloro-4-(1-piperazinyl)-2-quinolinamine are reacted to afford the product as a light yellow solid. LC-MS: 445 (M++1). 1H NMR (CDCl3) δ 7.70 (d, 1H), 7.60 (s, 1H), 7.15 (d, 1H), 6.02 (s, 1H), 4.70 (s, 2H), 4.22 (d, 1H), 4.10 (m, 1H), 3.92 (m, 1H), 3.60 (m, 4H), 3.10 (m, 6H), 2.25 (m, 1H), 2.15 (s, 3H), 1.60–1.90 (m, 3H), 1.30–1.40 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220856B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-9bfbcc2051b5444e8e28404cf1413249 |
| Source note | uspto-grants-2007_05 |