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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736646Generated: October 29, 2026

1-(2-Bromoethyl)-3-(trifluoromethoxy)benzene → 8-(2,5-Dimethoxy-phenylsulfanyl)-9-[2-(3-trifluoromethoxy-phenyl)-ethyl]-9H-purin-6-ylamine

https://huagongshe.com/reaction/736646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Bromoethyl)-3-(trifluoromethoxy)benzeneHCID 22929647—
ReactantHCID 178492621HCID 178492621—
Product8-(2,5-Dimethoxy-phenylsulfanyl)-9-[2-(3-trifluoromethoxy-phenyl)-ethyl]-9H-purin-6-ylamineHCID 5785052117%

Reaction Steps

The title compound was prepared from 8-(2,5-dimethoxy-phenylsulfanyl)-9H-purin-6-ylamine and. 1-(2-bromo-ethyl)-3-trifluoromethoxy-benzene by a procedure similar to examples 1 and 2. The compound was purified by preparative HPLC. 8-(2,5-Dimethoxy-phenylsulfanyl)-9-[2-(3-trifluoromethoxy-phenyl)-ethyl]-9H-purin-6-ylamine: Yield 17%, 1H NMR (CD3OD) δ 8.18 (s, 1H), 7.33 (t, J=8.0 Hz, 1H), 7.12-7.10 (m, 2H), 7.04-7.01 (m, 3H), 6.95 (bs, 1H), 4.57 (t, J=7.2 Hz, 2H), 3.75 (s, 3H), 3.74 (s, 3H), 3.24 (t, J=7.2 Hz, 2H); LC-MS [M+H]+ 492.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595401B2
Source datasetuspto-grants-2009_09
ORD IDord-0a804bb3b32a4342b5f6f74c49c8c768
Source noteuspto-grants-2009_09