Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433018Generated: November 1, 2026

MeOH tetrahydrofuran → (+/-)-1-(4-Amino-quinazolin-7-ylmethyl)-4-(6-chloro-benzo[b]thiophene-2-sulfonyl)-6-oxo-piperazine-2-carboxylic acid

https://huagongshe.com/reaction/1433018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMeOH tetrahydrofuranHCID 21899815—
Reactant(+/-)-1-(4-Amino-quinazolin-7-ylmethyl)-4-(6-chloro-benzo[b]thiophene-2-sulfonyl)-6-oxo-piperazine-2-carboxylic acid methyl esterHCID 54356203—
SolventWaterHCID 962—
Product(+/-)-1-(4-Amino-quinazolin-7-ylmethyl)-4-(6-chloro-benzo[b]thiophene-2-sulfonyl)-6-oxo-piperazine-2-carboxylic acidHCID 1798518975.2%

Reaction Steps

Water (1 mL) is added to a solution containing (±)-1-(4-amino-quinazolin-7-ylmethyl)-4-(6-chloro-benzo[b]thiophene-2-sulfonyl)-6-oxo-piperazine-2-carboxylic acid methyl ester (20 mg, 0.03 mmol), EXAMPLE 799, in a 1:1 mixture of THF/MeOH (2 mL). At ambient temperature, LiOH monohydrate (15 mg, 0.35 mmol) is then added. After 16 h, the reaction mixture is diluted with water and purified by reverse-phase HPLC [Buffer A: water w/0.1% TFA; Buffer B: CH3CN w/0.1% TFA; Gradient: 0% B to 60% B over 30 min] to provide 12 mg (63%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-93a6c16831f44c64a72a2e413dd34e89
Source noteuspto-grants-2009_11