HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzaldehyde → HCID 178520490, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | 6-Amino-1-hexanol | HCID 19960 | — |
| Reactant | Thiomorpholine | HCID 67164 | — |
| Reactant | 2,4-Dichlorobenzenethiol | HCID 70730 | — |
| Reactant | 2-Bromobenzenethiol | HCID 80598 | — |
| Reactant | 3-Chloro-4-fluorobenzaldehyde | HCID 593866 | — |
| Product | HCID 178520490 | HCID 178520490 | — |
Reaction Steps
The title compound was prepared by the procedures described in Example 1 substituting 2,4-dichlorothiophenol with 2-bromothiophenol, 2-chlorobenzaldehyde with 3-chloro-4-fluoro-benzaldehyde, and 6-amino-1-hexanol with thiomorpholine. 1H NMR (DMSO-d6, 300 MHz) δ 8.10 (d, J=1.5 Hz, 1H), 7.80 (d, J=8.5 Hz, 1H), 7.64 (dd, J=8.1, 1.5 Hz, 1H), 7.31-7.48 (m, 4H), 7.36 (m, 1H), 7.26 (dd, J=8.1, 1.8 Hz, 1H), 7.05 (d J=8.1 Hz, 1H), 3.96 (m, 2H), 3.82 (m, 2H), 2.62 (m, 4H). HRMS calculated for C19H17N1O1S2Br1Cl1: 455.9681. Observed: 455.9676.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06878700B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-7651976e77384669be87b60183ccaf39 |
| Source note | uspto-grants-2005_04 |