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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066483Generated: October 31, 2026

5-(2-Chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-hexahydro-pyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl ester → 7-(2-Chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-2,7-diaza-spiro[4.4]nonane-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2066483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-Chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-hexahydro-pyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl esterHCID 58117071—
Reactanttert-Butyl 2,7-diazaspiro[4.4]nonane-2-carboxylate hydrochlorideHCID 66870067—
Product7-(2-Chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-2,7-diaza-spiro[4.4]nonane-2-carboxylic acid tert-butyl esterHCID 58117086—

Reaction Steps

Prepared according to the method used in the preparation of 5-(2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-hexahydro-pyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl ester using 2,7-diaza-spiro[4.4]nonane-2-carboxylic acid tert-butyl ester hydrochloride in place of hexahydro-pyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl ester. The title compound was obtained as a pale yellow oil (96 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293735B2
Source datasetuspto-grants-2012_10
ORD IDord-d42eaed2b22c46bb8c57b11474774aac
Source noteuspto-grants-2012_10