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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066557Generated: November 2, 2026

Trifluoroacetic acid methylene chloride → 6-(2,7-Diaza-spiro[3.5]non-7-ylmethyl)-2-(6-fluoro-1H-indol-4-yl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/2066557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
Reactanttert-Butyl 2,7-diazaspiro[3.5]nonane-2-carboxylate hydrochlorideHCID 24820549—
Reactant2-(6-fluoro-1H-indol-4-yl)-6-[(5)-1-(hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)methyl]-4-morpholin-4-yl-thieno-[3,2-d]pyrimidineHCID 58117043—
Product6-(2,7-Diaza-spiro[3.5]non-7-ylmethyl)-2-(6-fluoro-1H-indol-4-yl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidineHCID 46239997—

Reaction Steps

Prepared according to the method used in the preparation of 2-(6-fluoro-1H-indol-4-yl)-6-[(S)-1-(hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)methyl]-4-morpholin-4-yl-thieno-[3,2-d]pyrimidine using 2,7-diaza-spiro[3.5]nonane-2-carboxylic acid tert-butyl ester hydrochloride in place of (S)-octahydro-pyrrolo[1,2-a]pyrazine, followed by BOC-deprotection using TFA:DCM (1:1). The title compound was obtained as a white solid (27 mg, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293735B2
Source datasetuspto-grants-2012_10
ORD IDord-fcebd5b7af4a4e4cb3b95177bc0b20a6
Source noteuspto-grants-2012_10