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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47578Generated: October 25, 2026

2,5-Difluorobenzaldehyde → (7bR,11aS)-N-(2,5-difluorobenzyl)-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/47578

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DifluorobenzaldehydeHCID 137663—
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-(2,5-difluorobenzyl)-1,2,7b,8,9,10,11,11a-octahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indol-6-amineHCID 60071802—

Reaction Steps

Using 2,5-difluorobenzaldehyde 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 159. 1H NMR(CDCl3) δ: 7.05-6.98 (m, 1H), 6.97-6.90 (m, 1H), 6.90-6.80 (m, 1H), 6.26 (d, 1H, J=2.5 Hz), 6.14 (d, 1H, J=2.2 Hz), 4.23 (broad s, 2H), 3.59 (ABq, 2H), 3.50-3.40 (m, 1H), 3.30-3.17 (m, 2H), 3.05-2.65 (m, 6H), 2.51 (dd, 1H, J=12.7, 9.5 Hz), 1.92-1.78 (m, 2H). LRMS (ES)+: 388.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699852B2
Source datasetuspto-grants-2004_03
ORD IDord-5fd6fab9a5ea4c578eed07dceccb1c4a
Source noteuspto-grants-2004_03