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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893640Generated: October 25, 2026

Sulfamic acid 1-isopropyl-cyclopropyl ester → 2-[2-Ethyl-1-(1-isopropyl-cyclopropoxysulfonylaminocarbonyl)-cyclopropylcarbamoyl]-4-(6-methoxy-isoquinolin-1-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1893640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamic acid 1-isopropyl-cyclopropyl esterHCID 57785237—
Reactant2-(1-Carboxy-2-ethyl-cyclopropylcarbamoyl)-4-(6-methoxy-isoquinolin-1-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 68795564—
Product2-[2-Ethyl-1-(1-isopropyl-cyclopropoxysulfonylaminocarbonyl)-cyclopropylcarbamoyl]-4-(6-methoxy-isoquinolin-1-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 76605113—

Reaction Steps

2-[2-Ethyl-1-(1-isopropyl-cyclopropoxysulfonylaminocarbonyl)-cyclopropylcarbamoyl]-4-(6-methoxy-isoquinolin-1-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester was prepared according to the method presented in Example 27. Treatment of 2-(1-carboxy-2-ethyl-cyclopropylcarbamoyl)-4-(6-methoxy-isoquinolin-1-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.50 mmol) occurred under the same conditions, adjusted for scale with the exception of utilizing sulfamic acid 1-isopropyl-cyclopropyl ester to afford acylsulfamate (185 mg, 56%): LCMS found 660.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513186B2
Source datasetuspto-grants-2013_08
ORD IDord-92d84ae1d3ce44b582e0be31588fa30d
Source noteuspto-grants-2013_08