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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208194Generated: November 2, 2026

rac-tert-butyl (3R,4R)-4-amino-3-hydroxypiperidine-1-carboxylate → tert-Butyl(3S*,4S*)-4-{[(4-[2-(cyclopropylmethoxy)-4-fluorophenyl]-6-methyl-5-{[2-(trimethylsilyl)ethoxy]methyl}-5H-pyrrolo[3,2-d]pyrimidin-7-yl)carbonyl]amino}-3-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/2208194

Reaction equation

Participants

RoleNameHCIDCharge
Reactantrac-tert-butyl (3R,4R)-4-amino-3-hydroxypiperidine-1-carboxylateHCID 10727458—
Reactant4-[2-(cyclopropylmethoxy)-4-fluorophenyl]-6-methyl-5-{[2-(trimethylsilyl)ethoxy]methyl}-5H-pyrrolo[3,2-d]pyrimidine-7-carboxylic acidHCID 67956161—
Producttert-Butyl(3S*,4S*)-4-{[(4-[2-(cyclopropylmethoxy)-4-fluorophenyl]-6-methyl-5-{[2-(trimethylsilyl)ethoxy]methyl}-5H-pyrrolo[3,2-d]pyrimidin-7-yl)carbonyl]amino}-3-hydroxypiperidine-1-carboxylateHCID 67033425—

Reaction Steps

Starting from 4-[2-(cyclopropylmethoxy)-4-fluorophenyl]-6-methyl-5-{[2-(trimethylsilyl)ethoxy]methyl}-5H-pyrrolo[3,2-d]pyrimidine-7-carboxylic acid (example D.c2) and tert-butyl (3R*,4R*)-4-amino-3-hydroxy-piperidine-1-carboxylate (example C2) the title compound is obtained as pale yellow viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376442B2
Source datasetuspto-grants-2016_06
ORD IDord-91e99b5a686d4bf0b5a57b975827f2a1
Source noteuspto-grants-2016_06