HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chlorobenzyl alcohol → HCID 69732063, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chlorobenzyl alcohol | HCID 70117 | — |
| Reactant | 1-Boc-4-(3-amino-6-bromopyrazin-2-YL)piperazine | HCID 46864072 | — |
| Product | HCID 69732063 | HCID 69732063 | — |
Reaction Steps
3′-Amino-6′-(3-chloro-benzyloxy)-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-carboxylic acid tert-butyl ester I-3s was prepared from 3′-Amino-6′-bromo-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-carboxylic acid tert-butyl ester I-3r (1.0 g, 2.8 mmol) and 3-chlorobenzyl alcohol (0.36 mL, 3.1 mmol) in a manner analogous to compound I-1b in example 1. The title compound I-3s was obtained as a red viscous oil (394 mg, 34% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06894050B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-bda0202bfd5e46c7b8b74870fd7a8d7d |
| Source note | uspto-grants-2005_05 |