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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506743Generated: October 25, 2026

9-(1-Isopropyl-piperidin-4-yloxy)-2,3,4,5-tetrahydro-[1,4]diazepino[1,2-a]indol-1-one → 5-Benzyloxy-1-(2-tert-butoxycarbonylamino-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/506743

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-(1-Isopropyl-piperidin-4-yloxy)-2,3,4,5-tetrahydro-[1,4]diazepino[1,2-a]indol-1-oneHCID 16679701—
Reactant3-Boc-1,2,3-oxathiazolidine 2,2-dioxideHCID 23584020—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant5-Benzyloxy-pyrrolo[2,3-b]pyridine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl esterHCID 68423305—
Product5-Benzyloxy-1-(2-tert-butoxycarbonylamino-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl esterHCID 68463351—

Reaction Steps

The title compound was synthesized in analogy to example 1, intermediate b), from 5-benzyloxy-pyrrolo[2,3-b]pyridine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (intermediate M), 2,2-dioxo-[1,2,3]oxathiazolidine-3-carboxylic acid tert-butyl ester (prepared according to WO02/072584) and potassium tert-butoxide, to give the product as a colorless foam (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786109B2
Source datasetuspto-grants-2010_08
ORD IDord-3c467e8463d44f4399ddf5b13177d774
Source noteuspto-grants-2010_08