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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661101Generated: November 1, 2026

Boronic Acid → tert-Butyl (5-bromo-4-cyclopropyl-1,3-thiazol-2-yl)carbamate

https://huagongshe.com/reaction/661101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoronic AcidHCID 61668—
ReactantHCID 57634141HCID 57634141—
ReactantHCID 86635458HCID 86635458—
Producttert-Butyl (5-bromo-4-cyclopropyl-1,3-thiazol-2-yl)carbamateHCID 45117858—
ProductHCID 57634141HCID 57634141—

Reaction Steps

Example 170, N—((S)-2-amino-3-(6-trifluoromethyl)pyridine-3-yl)propyl)-5-(isoquinolin-6-yl)thiazol-2-amine: The title compound was synthesized in a manner similar to that described for Example 81 using (S)-tert-butyl 1-(5-bromothiazol-2-yl-(Boc)-amino)-3-(6-(trifluoromethyl)pyridin-3-yl)propan-2-ylcarbamate to couple with the boronic acid. (S)-tert-butyl 1-(5-bromothiazol-2-yl-(Boc)-amino)-3-(6-(trifluoromethyl)pyridin-3-yl)propan-2-ylcarbamate was synthesized as shown in Scheme 39. Theoretical (M+H) 430.4 found 430.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084479B2
Source datasetuspto-grants-2011_12
ORD IDord-5e4915fb0d454881b8486f5e9355e377
Source noteuspto-grants-2011_12