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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37360Generated: October 27, 2026

Ammonium Chloride → 10-[(2-Bromo-5-pyridinyl)methyl]-8-chloro-10,11-dihydrodibenz[b,f][1,4]oxazepine

https://huagongshe.com/reaction/37360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-5-(chloromethyl)pyridineHCID 6424658—
Reactant8-Chloro-10,11-dihydrodibenzo[b,f][1,4]oxazepineHCID 15229227—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product10-[(2-Bromo-5-pyridinyl)methyl]-8-chloro-10,11-dihydrodibenz[b,f][1,4]oxazepineHCID 1578068580.7%

Reaction Conditions

Temperature-23 °C

Reaction Steps

To a stirred solution of 8-chloro-10,11-dihydrodibenz[b,f][1,4]oxazepine (2 g) in THF (25 mL) at -78° C. was added 1.6 M hexane solution of n-butyl lithium (5.4 mL). After 25 minutes, 3-chloromethyl-6-bromopyridine (1.79 g) in THF (5 mL) was added. After 30 minutes, the temperature was raised to -23° C. After 30 minutes, an excess saturated solution of NH4Cl was added and the mixture was extracted with ether. The organic extract was dried over MgSO4 and concentrated. The residue was chromatographed over silica gel using 10% ethyl acetate in hexane as eluant. Appropriate fractions were pooled to give the title compound (2.8 g) as a thick gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420270
Source datasetuspto-grants-1995_05
ORD IDord-9ffddc0596474edc81dec07df29cf66a
Source noteuspto-grants-1995_05