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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923931Generated: October 30, 2026

(S)-3-N-Boc-aminomethyl pyrrolidine → (R)-tert-butyl ((1-(3-bromo-5-((4-(trifluoromethoxy)phenyl)carbamoyl)pyridin-2-yl)pyrrolidin-3-yl)methyl)carbamate

https://huagongshe.com/reaction/923931

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-3-N-Boc-aminomethyl pyrrolidineHCID 1519426—
Reactant5-bromo-6-chloro-N-(4-(trifluoromethoxy)phenyl)nicotinamideHCID 86702595—
Product(R)-tert-butyl ((1-(3-bromo-5-((4-(trifluoromethoxy)phenyl)carbamoyl)pyridin-2-yl)pyrrolidin-3-yl)methyl)carbamateHCID 118198938—

Reaction Steps

The title compound was prepared in an analogous fashion to that described in Stage 93.1 using 5-bromo-6-chloro-N-(4-(trifluoromethoxy)phenyl)nicotinamide (Stage 12.2) and (S)-tert-butyl (pyrrolidin-3-ylmethyl)carbamate. LC-MS (Condition 6) tR=2.7 min, m/z=559.0/561.0 [M+H]+, m/z=581.0 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278981B2
Source datasetuspto-grants-2016_03
ORD IDord-f51f6644befd40549a4906329806caaa
Source noteuspto-grants-2016_03