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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471847Generated: October 30, 2026

4-(tert-Butoxycarbonylaminomethyl)phenylboronic acid → HCID 57733014, compound

https://huagongshe.com/reaction/1471847

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(tert-Butoxycarbonylaminomethyl)phenylboronic acidHCID 3863163—
ReactantN-(1-Bromoisoquinolin-3-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamideHCID 57732996—
ProductHCID 57733014HCID 57733014—

Reaction Steps

tert-Butyl 4-(3-(1-(2,2-difluorobenzo[d][,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzylcarbamate was made by the procedure shown above starting from N-(1-bromoisoquinolin-3-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide and 4-((tert-butoxycarbonylamino)methyl)phenylboronic acid. ESI-MS m/z calc. 573.2. found 574.3 (M+1)+. Retention time 2.26 minutes. 1H NMR (400 MHz, DMSO-d6) δ 8.94 (s, 1H), 8.40 (s, 1H), 7.97 (d, J=8.2 Hz, 1H), 7.86 (d, J=8.6 Hz, 1H), 7.74-7.70 (m, 1H), 7.61 (d, J=1.2 Hz, 1H), 7.54-7.38 (m, 8H), 4.22 (d, J=5.9 Hz, 2H), 1.57-1.55 (m, 2H), 1.41 (s, 9H), 1.22-1.20 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012473B2
Source datasetuspto-grants-2015_04
ORD IDord-baf387ed25f74a49b308752cefe0d35a
Source noteuspto-grants-2015_04