Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23293Generated: October 25, 2026

2-(Trifluoromethoxy)benzaldehyde → (7bR,11aS)-N-[2-(trifluoromethoxy)benzyl]-1,2,7b,8,9,10,11,11a-octahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indol-6-amine

https://huagongshe.com/reaction/23293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethoxy)benzaldehydeHCID 2777192—
Reactanttert-butyl (7bR,11aS)-6-amino-1,2,7b,10,11,11a-hexahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indole-9(8H) carboxylateHCID 86586437—
Product(7bR,11aS)-N-[2-(trifluoromethoxy)benzyl]-1,2,7b,8,9,10,11,11a-octahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indol-6-amineHCID 60071870—

Reaction Steps

Using 2-(trifluoromethoxy)benzaldehyde and following the procedures described in EXAMPLE 126, tert-butyl (7bR,11aS)-6-amino-1,2,7b,10,11,11a-hexahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indole-9(8H)-carboxylate from EXAMPLE 33, Part B was converted into the title compound of EXAMPLE 165. LRMS (ES)+: 436.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849619B2
Source datasetuspto-grants-2005_02
ORD IDord-7742cf67d29c4a4abad20459971de61d
Source noteuspto-grants-2005_02