HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 59699568, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | HCID 69216352 | HCID 69216352 | — |
| Product | HCID 59699568 | HCID 59699568 | — |
Reaction Steps
This compound was prepared from 6-chloro-4-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carboxylic acid ethyl ester (82) and 2-bromoacetophenone according to General Procedure B. Yield 333 mg (59%), MP 227° C.; 1H-NMR (DMSO-d6): δ 1.29 (t, J=7.2 Hz, 3H), 3.20 (m, 4H), 3.92 (m, 4H), 4.32 (q, J=7.2 Hz, 2H), 5.87 (s, 2H), 7.17 (dd, J=3.6, 4.8 Hz, 1H), 7.48 (dd, J=1.2, 3.6 Hz, 1H), 7.61 (m, 2H), 7.73 (m, 1H), 7.81 (dd, J=1.2, 4.8 Hz, 1H), 8.11 (m, 2H), 8.32 (d, J=2.6 Hz, 1H), 8.64 (d, J=2.8 Hz, 1H); EIMS: 565 (M+1). Anal. (C28H25ClN4O5S) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361760B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-4e56b10a542746f48c5f0d238abbaed5 |
| Source note | uspto-grants-2008_04 |