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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066471Generated: October 30, 2026

tert-Butyl 1-oxa-4,9-diazaspiro(5.5)undecane-4-carboxylate → 9-(2-Chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-1-oxa-4,9-diaza-spiro[5.5]undecane-4-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2066471

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 1-oxa-4,9-diazaspiro(5.5)undecane-4-carboxylateHCID 53439217—
Reactant4-(2-Chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-1-oxa-4,9-diaza-spiro[5.5]undecane-9-carboxylic acid tert-butyl esterHCID 58117135—
Product9-(2-Chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-1-oxa-4,9-diaza-spiro[5.5]undecane-4-carboxylic acid tert-butyl esterHCID 58117065—

Reaction Steps

Prepared according to the method used in the preparation of 4-(2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-1-oxa-4,9-diaza-spiro[5.5]undecane-9-carboxylic acid tert-butyl ester using 1-oxa-4,9-diaza-spiro[5.5]undecane-4-carboxylic acid tert-butyl ester in place of 4-ethoxy-4-methylaminomethyl-piperidine-1-carboxylic acid tert-butyl ester. The title compound was obtained as a white solid (110 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293735B2
Source datasetuspto-grants-2012_10
ORD IDord-d4d75730d1ab4577a291062de308ace6
Source noteuspto-grants-2012_10