HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-(tert-Butyldimethylsilyloxy)ethyl)methylamine → HCID 178484770, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-(tert-Butyldimethylsilyloxy)ethyl)methylamine | HCID 16203640 | — |
| Reactant | HCID 178484773 | HCID 178484773 | — |
| Reactant | HCID 178524871 | HCID 178524871 | — |
| Product | HCID 178484770 | HCID 178484770 | 47.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045486B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-73fc3cbd83ad4c608dcab39076166c07 |
| Source note | uspto-grants-2015_06 |