Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16168Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 86599876, compound

https://huagongshe.com/reaction/16168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactanttrans-N-(8-Amino-7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamideHCID 86599875—
SolventDichloromethaneHCID 6344—
ProductHCID 86599876HCID 8659987643.5%

Reaction Conditions

Temperature35 °C

Reaction Steps

Benzenesulfonyl chloride (10 μL, 0.08 mmol) was added under N2 to trans-N-(8-amino-7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide (5.0 mg, 0.01 mmol) in 1 mL of CH2Cl2 and 2 μL (1.1 eq) of triethylamine. The resulting mixture was stirred at 35° C. for 4 h. After cooling the mixture was evaporated and the crude compound was purified by chromatography on silica. Elution with toluene/ethyl acetate 1:0→0:1 (gradient) gave trans-N-(7-chloro-2,3,4,14b-tetrahydro-8-[(phenylsulfonyl)amino]-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide (2.4 mg, 32%). Data: (m/z)=552 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737136B2
Source datasetuspto-grants-2010_06
ORD IDord-91e5ece05cce47edb5e010e8dc3c86d3
Source noteuspto-grants-2010_06