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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266029Generated: November 2, 2026

Hydroxyamine hydrochloride → HCID 86758921, compound

https://huagongshe.com/reaction/1266029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 86758922HCID 86758922—
SolventPyridineHCID 1049—
ProductHCID 86758921HCID 8675892192.3%

Reaction Steps

Hydroxylamine hydrochloride (0.10 g, 0.325 mmol) was added to a solution of 6-(4-fluoro-phenyl)-1-oxo-1,2,3,4-tetrahydro-[1,4]diazepino[6,7,1-hi]indole-7-carbaldehyde (56.0 mg, 0.813 mmol) in pyridine (10 mL) and stirred at rt for 20 h. Upon consumption of the aldehyde as indicated by TLC, the solvent was removed in vacuo. The residue was taken up in 2N HCl and extracted with EtOAc several times. The combined organic extracts were dried over anhydrous MgSO4 and concentrated to give 97 mg (92%) of a pale-yellow solid: mp 277-279° C.; 1H NMR (DMSO-d6) δ 3.50 (br s, 2H), 4.12-4.14 (m, 2H), 7.30 (t, 1H, J=6.0 Hz), 7.43 (t, 2H, J=9.0 Hz), 7.57-7.62 (m, 2H), 7.89 (s, 1H), 7.94 (d, 1H, J=9.0 Hz), 8.33 (d, 1H, J=6.0 Hz), 8.41 (t, 1H, J=6.0 Hz), 10.80 (s, 1H). HRMS calcd. for C18H14N3O2F 323.1070 (M+), found 323.1066.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548494B1
Source datasetuspto-grants-2003_04
ORD IDord-a309f3079c4443c0a76296ecc1437e8c
Source noteuspto-grants-2003_04