Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876361Generated: October 31, 2026

4-Chlorophenol → HCID 131732587, compound

https://huagongshe.com/reaction/876361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorophenolHCID 4684—
ReactantHCID 68502906HCID 68502906—
ReactantHCID 131732588HCID 131732588—
ProductHCID 131732587HCID 131732587—

Reaction Steps

This compound was prepared from (−)-2-methyl-8-(pyridazin-3-yl)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-5-ol from Step H in Example 1 and 4-chlorophenol, following the procedures of Steps J and K in Example 1. (+)-5-(4-Chlorophenyl)-8-(pyridazin-3-yl)-2,3,4,5-tetrahydro-1H-benzo[c]azepine, tartrate salt (AUC HPLC>99%) is a white solid: mp 106-108° C.; 1H NMR (CD3OD, 500 MHz) δ 9.18 (d, J=5.0 Hz, 1H), 8.20-8.17 (m, 2H), 8.07 (d, J=8.0 Hz, 1H), 7.80 (dd, J=8.7, 3.8 Hz, 1H), 7.66 (d, J=7.9 Hz, 1H), 7.25 (d, J=9.0 Hz, 2H), 7.05 (d, J=9.0 Hz, 2H), 5.73 (d, J=7.6 Hz, 1H), 4.92-4.84 (m, 1H), 4.52-4.46 (m, 1H), 4.42 (s, 3H), 3.90-3.80 (m, 1H), 3.56-3.50 (m, 1H), 2.86 (s, 3H), 2.46-2.37 (m, 2H); ESI MS m/z 366 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987252B2
Source datasetuspto-grants-2015_03
ORD IDord-8ed3fba374d24601aa62a615edf79385
Source noteuspto-grants-2015_03