HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-((tert-butyldimethylsilyl)oxy)ethyl)propan-2-amine → HCID 178457484, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-((tert-butyldimethylsilyl)oxy)ethyl)propan-2-amine | HCID 57917054 | — |
| Reactant | HCID 178484773 | HCID 178484773 | — |
| Reactant | HCID 178524878 | HCID 178524878 | — |
| Product | HCID 178457484 | HCID 178457484 | 38.2% |
Reaction Steps
5-Benzyloxy-2-biphenyl-2-ylmethyl-6-hydroxypyrimidine-4-carboxylic acid [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-isopropylamide (9-03) (1.7 g, 38.16%) was synthesized as a dark liquid from 5-benzyloxy-2-biphenyl-2-ylmethyl-6-hydroxypyrimidine-4-carboxylic acid (7-01) (3 g, 7.28 mmol) and [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-isopropyl amine (8-b) (1.73 g, 8.01 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-7f475d719b53474092b0ee0f4bc09095 |
| Source note | uspto-grants-2015_06 |