Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908646Generated: October 30, 2026

Diisopropylethylamine → (R)-4-(7-chloro-5-trifluoromethyl-thiazolo[4,5-d]pyrimidin-2-yl)-1-(4-cyclopropyl-benzenesulfonyl)-piperazine-2-carboxylic acid 4-trifluoromethoxy-benzylamide

https://huagongshe.com/reaction/908646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(R)-1-(4-cyclopropyl-benzenesulfonyl)-piperazine-2-carboxylic acid 4-trifluoromethoxy-benzylamideHCID 59703776—
Reactant2,7-Dichloro-5-trifluoromethyl-thiazolo[4,5-d]pyrimidineHCID 59703826—
SolventChloroformHCID 6212—
Product(R)-4-(7-chloro-5-trifluoromethyl-thiazolo[4,5-d]pyrimidin-2-yl)-1-(4-cyclopropyl-benzenesulfonyl)-piperazine-2-carboxylic acid 4-trifluoromethoxy-benzylamideHCID 59703751102.9%

Reaction Steps

To a mixed solution of the compound (27 mg) obtained in Example 1001, Step 8, the compound (43 mg) obtained in Step 4 and chloroform (0.50 ml) was added N,N-diisopropylethylamine (19 μl) under ice-cooling. After stirring overnight at room temperature, the reaction mixture was purified by silica gel column chromatography (chloroform:methanol=20:1) to give the title compound (66 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017612B2
Source datasetuspto-grants-2011_09
ORD IDord-cac53cd31eef4af38e6687a0f06992ca
Source noteuspto-grants-2011_09