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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169284Generated: November 2, 2026

N-(2-((tert-butyldimethylsilyl)oxy)ethyl)propan-2-amine → HCID 178457477, compound

https://huagongshe.com/reaction/2169284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-((tert-butyldimethylsilyl)oxy)ethyl)propan-2-amineHCID 57917054—
ReactantHCID 178457482HCID 178457482—
ReactantHCID 178524870HCID 178524870—
ProductHCID 178457477HCID 17845747752.55%

Reaction Steps

5-Benzyloxy-6-hydroxy-2-[1-(4-trifluoromethyl-phenyl)-cyclopentylmethyl]-pyrimidine-4-carboxylic acid [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-isopropylamide (245) (187 mg, 52.55%) as a yellow sticky solid was synthesized from 5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethyl-phenyl)-cyclopentylmethyl]-pyrimidine-4-carboxylic acid (244) (250 mg, 0.53 mmol) and 2-(tert-butyl-dimethylsilanyloxy)-ethyl]-isopropylamine (8b) following the procedure as described for 5-benzyloxy-2-[1-(2,5-dichlorophenyl)-cyclopentylmethyl]-6-hydroxypyrimidine-4-carboxylic acid [2-(tert-butyl-dimethylsilanyloxy)-ethyl]isopropylamide (206).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-8a6083c9aa2c455db70ff883f60e4bea
Source noteuspto-grants-2015_06