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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607267Generated: October 29, 2026

4-[2-Amino-4-(3-bromo-benzyloxy)-phenylsulfanyl]-phenol → 4-[4-(4-Bromo-benzyloxy)-2-(2-methylsulfanyl-thiazolo[4,5-d]pyrimidin-7-ylamino)-phenylsulfanyl]-phenol

https://huagongshe.com/reaction/607267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[2-Amino-4-(3-bromo-benzyloxy)-phenylsulfanyl]-phenolHCID 66808268—
Reactant4-[2-Amino-4-(4-bromo-benzyloxy)-phenylsulfanyl]-phenolHCID 66808289—
ReactantN'-(5-Cyano-2-methylsulfanyl-thiazol-4-yl)-N,N-dimethyl-formamidineHCID 66808347—
Product4-[4-(4-Bromo-benzyloxy)-2-(2-methylsulfanyl-thiazolo[4,5-d]pyrimidin-7-ylamino)-phenylsulfanyl]-phenolHCID 6680846527%

Reaction Steps

A solution of the product from Example 167A and the product from Example 16A were reacted according to the procedure from Example 167B substituting the product from Example 16A for the product from Example 15A to provide the crude material which was purified by trituration with methanol to provide the title compound as a white solid (46 mg, 27%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 2.76 (s, 3H), 5.09 (s, 2H), 6.70 (d, J=8.46 Hz, 2H), 6.91-7.24 (m, 5H), 7.38 (d, J=8.09 Hz, 2H), 7.56 (d, J=8.09 Hz, 2H), 8.46 (s, 1H), 9.71 (s, 2H); MS (ESI)+ m/z 583/585 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915411B2
Source datasetuspto-grants-2011_03
ORD IDord-8ee15170f6fb4b46a998c0ecd9f56ee1
Source noteuspto-grants-2011_03