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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 2-((((9h-fluoren-9-yl)methoxy)carbonyl)amino)-4-bromothiophene-3-carboxylate | HCID 68756520 | — |
| Solvent | DCM morpholine | HCID 20307284 | — |
| Product | Methyl 2-amino-4-bromothiophene-3-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073891B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-f55ac2d5a5fa4c6485b5f89d2cf7bd6d |
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| Source note | uspto-grants-2015_07 |
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