Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025564Generated: October 30, 2026

2-Bromo-1,3-thiazole-4-carboxamide → HCID 71008577, compound

https://huagongshe.com/reaction/1025564

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1,3-thiazole-4-carboxamideHCID 45789632—
Reactant2-(6-(tert-Butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl acetateHCID 59473769—
ProductHCID 71008577HCID 7100857710%

Reaction Steps

This compound was prepared with the same method as described in Example 1 by using 2-bromothiazole-4-carboxylic acid amide (intermediate-2) and acetic acid 2-(6-tert-butyl-8-fluoro-1-oxo-1H-phthalazin-2-yl)-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl ester (intermediate 5). The desired compound was prepared in two steps (10% yield). 1H NMR (300 MHz, DMSO-d6) δ 8.59 (d, J=2.4 Hz, 1H), 8.46 (s, 1H), 7.94 (d, J=1.8 Hz, 1H), 7.88-7.79 (m, 2H), 7.66-7.63 (m, 2H), 4.61-4.52 (m, 2H), 1.46 (s, 9H). LC-MS calcd for C23H21FN4O3S 452.13, obsd 453 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729078B2
Source datasetuspto-grants-2014_05
ORD IDord-ba11c025a60a47b186930688578a8e50
Source noteuspto-grants-2014_05