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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169163Generated: October 26, 2026

N-(2-(tert-Butyldimethylsilyloxy)ethyl)methylamine → HCID 178484770, compound

https://huagongshe.com/reaction/2169163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-(tert-Butyldimethylsilyloxy)ethyl)methylamineHCID 16203640—
ReactantHCID 178484773HCID 178484773—
ReactantHCID 178524871HCID 178524871—
ProductHCID 178484770HCID 17848477047.9%

Reaction Steps

5-Benzyloxy-2-[1-(4-chlorophenyl)-cyclopentylmethyl]-6-hydroxypyrimidine-4-carboxylic acid [2-(tert-butyl-dimethylsilanyloxy)-ethyl]methyl-amide (29-02) (2 g, 47.85%) was synthesized from 5-benzyloxy-2-[1-(4-chlorophenyl)-cyclopentylmethyl]-6-hydroxypyrimidine-4-carboxylic acid (28-02) (3 g, 6.84 mmol) and [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-methyl-amine (8-a) as a gummy solid (1.4 g, 7.53 mmol) following the procedure as described for 5-benzyloxy-2-biphenyl-2-ylmethyl-6-hydroxypyrimidine-4-carboxylic acid [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-methyl-amide (9-01).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-73fc3cbd83ad4c608dcab39076166c07
Source noteuspto-grants-2015_06