HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(N-tert-Butoxycarbonyl-N-methylamino)pyrrolidine → Hydrochloric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(N-tert-Butoxycarbonyl-N-methylamino)pyrrolidine | HCID 2761404 | — |
| Reactant | (S)-Methyl-pyrrolidin-3-yl-carbamic acid tert-butyl ester | HCID 7171888 | — |
| Reactant | 4-Bromo-5-isoquinolinesulfonyl chloride | HCID 14580058 | — |
| Reactant | 4-Methylisoquinoline-5-sulfonyl chloride | HCID 15487110 | — |
| Reactant | HCID 67243666 | HCID 67243666 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 67242245 | HCID 67242245 | — |
Reaction Steps
3-[N-(tert-Butoxycarbonyl)-N-methylamino]-1-(4-methyl-5-isoquinoline sulfonyl)pyrrolidine (Intermediate 23) can be prepared by using 4-methyl-5-isoquinolinesulfonyl chloride and 3-[N-(tert-butoxycarbonyl)-N-methyl-amino]pyrrolidine in the method of Example 1-3, Step A instead of 4-bromo-5-isoquinolinesulfonyl chloride and (S)-3-[N-(tert-butoxycarbonyl)-N-methyl-amino]pyrrolidine, respectively, and then used in the method of Step B in a similar manner to obtain the title compound as hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415372B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-c950ad85523c45dfa5fb980851cce081 |
| Source note | uspto-grants-2013_04 |