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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519781Generated: October 26, 2026

Methyl 2-((((9h-fluoren-9-yl)methoxy)carbonyl)amino)-4-bromothiophene-3-carboxylate → Methyl 2-amino-4-bromothiophene-3-carboxylate

https://huagongshe.com/reaction/1519781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-((((9h-fluoren-9-yl)methoxy)carbonyl)amino)-4-bromothiophene-3-carboxylateHCID 68756520—
SolventDCM morpholineHCID 20307284—
ProductMethyl 2-amino-4-bromothiophene-3-carboxylateHCID 68754257—

Reaction Steps

Methyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-bromothiophene-3-carboxylate (1 g) was stirred in DCM/morpholine (12 mL, 1:1) at rt until all the ester was consumed. The crude mixture was concentrated under reduced pressure. The residue was dissolved in ethyl ether. The white solid was removed. The mother liquid was concentrated under reduced pressure and a 1:1 mixture of ethyl ether/pentane (20 mL) was added. An additional white solid was removed. The organic layer was concentrated under reduced pressure and the crude mixture was placed under high vacumn to remove the excess of morpholine. The crude amine was taken directly to the next reaction step without further purification. Method[1], MS(ESI) 235.9 [M+H], Retention time=1.919 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073891B2
Source datasetuspto-grants-2015_07
ORD IDord-f55ac2d5a5fa4c6485b5f89d2cf7bd6d
Source noteuspto-grants-2015_07