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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270853Generated: October 31, 2026

Bromine → Tert-butyl 4-(4-amino-7-bromothieno[3,2-c]pyridin-3-yl)phenylcarbamate

https://huagongshe.com/reaction/1270853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantTert-butyl 4-(4-aminothieno[3,2-c]pyridin-3-yl)phenylcarbamateHCID 18451468—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(4-amino-7-bromothieno[3,2-c]pyridin-3-yl)phenylcarbamateHCID 1845145995.7%

Reaction Steps

A solution of bromine (0.4 mL, 4.6 mmol) in dichloromethane (5 mL) was added dropwise to a −5° C. solution of Example 76A (1.57 g, 4.6 mmol) in dichloromethane (30 mL). The mixture was stirred at −5° C. to 0° C. for 15 minutes and quenched with 1:1 saturated NaHCO3 and saturated NaHSO3 (10 mL). The organic phase was separated, washed with water and brine, dried (NaSO4), filtered, and concentrated to provide 1.85 g of the desired product. MS (ESI(+)) m/e 421 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202363B2
Source datasetuspto-grants-2007_04
ORD IDord-442b5d6be6b44dc7bc889be218babab6
Source noteuspto-grants-2007_04