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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857770Generated: October 30, 2026

1-((Tert-butoxy)carbonyl)-3,3-dimethylpyrrolidine-2-carboxylic acid → 1-(tert-butoxycarbonyl)-3,3-dimethylprolyl-N-[5-chloro-2-(1H-tetraazol-yl)-benzyl]-L-prolinamide

https://huagongshe.com/reaction/857770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((Tert-butoxy)carbonyl)-3,3-dimethylpyrrolidine-2-carboxylic acidHCID 4059597—
ReactantN-[5-chloro-2-(1H-tetraazol-1-yl)benzyl]-L-prolinamideHCID 69655818—
Solvent1,2-DichloroethaneHCID 11—
Product1-(tert-butoxycarbonyl)-3,3-dimethylprolyl-N-[5-chloro-2-(1H-tetraazol-yl)-benzyl]-L-prolinamideHCID 69656113—

Reaction Steps

The title compound was prepared as a mixture of diastereomers from 1-(tert-butoxycarbonyl)-3,3-dimethyl-dl-proline (61 mg, 0.25 mmol) and N-[5-chloro-2-(1H-tetrazol-1-yl)benzyl]-L-prolinamide (Example 26, Step B, 95 mg, 0.25 mmol) essentially according to the EDC coupling procedure described in Example 39, Step D. The diastereomeric products were separated by reverse phase HPLC and were carried on directly to deprotection.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144899B2
Source datasetuspto-grants-2006_12
ORD IDord-4694cd1689aa47b68449eee806b6c3ae
Source noteuspto-grants-2006_12