HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl methyl((3R)-pyrrolidin-3-yl)carbamate → Hydrochloric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl methyl((3R)-pyrrolidin-3-yl)carbamate | HCID 7019173 | — |
| 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 57811271 | HCID 57811271 | — |
Reaction Steps
3-[N-(tert-Butoxycarbonyl)-N-methylamino]-1-(4-methyl-5-isoquinolinesulfonyl)pyrrolidine (Intermediate 23b) can be prepared by using 4-methyl-5-isoquinolinesulfonyl chloride and (R)-3-[N-(tert-butoxycarbonyl)-N-methylamino]pyrrolidine in the method of Example 1-3, Step A instead of 4-bromo-5-isoquinolinesulfonyl chloride and (S)-3-[N-(tert-butoxycarbonyl)-N-methylamino]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 | US07964613B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-6f8ac68ffa1d4b3fb22ab5bec225bc34 |
| Source note | uspto-grants-2011_06 |