HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-((tert-butyldimethylsilyl)oxy)ethyl)propan-2-amine → HCID 178457477, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-((tert-butyldimethylsilyl)oxy)ethyl)propan-2-amine | HCID 57917054 | — |
| Reactant | HCID 178457482 | HCID 178457482 | — |
| Reactant | HCID 178524870 | HCID 178524870 | — |
| Product | HCID 178457477 | HCID 178457477 | 52.55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045486B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-8a6083c9aa2c455db70ff883f60e4bea |
| Source note | uspto-grants-2015_06 |