HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 66727301, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | N-(tert-butoxycarbonyl)-2-aminoethanethiol | HCID 3017761 | — |
| Reactant | HCID 66727336 | HCID 66727336 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66727301 | HCID 66727301 | — |
Reaction Steps
320 mg of (S)-6-(4-tert-butoxycarbonyl-2-methyl-1,4-diazepan-1-ylsulfonyl)isoquinoline 2-oxide was dissolved in dichloromethane, and 0.1 mL of ethyl chlorocarbonate, 0.42 mL of 2-(N-tert-butoxycarbonylamino)ethanethiol, and 0.21 mL of triethylamine were added at 0° C. The reaction solution was stirred at room temperature for 16 hours and then concentrated under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (hexane:acetone=4:1) to obtain 223 mg of the compound of interest as a colorless oil (51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08951997B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-6090e760212e40269a29ad6e686bfa9c |
| Source note | uspto-grants-2015_02 |