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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716538Generated: October 31, 2026

2,5-Dibromothieno(3,2-b)thiophene → [(S)-1-((S)-2-{5-[4-(5-bromo-thieno[3,2-b]thiophen-2-yl)-phenyl]-1H-imidazol-2-yl}-pyrrolidine-1-carbonyl)-2-methyl-propyl]-carbamic acid methyl ester

https://huagongshe.com/reaction/716538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dibromothieno(3,2-b)thiopheneHCID 3597455—
ReactantMethyl ((S)-3-methyl-1-oxo-1-((S)-2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)pyrrolidin-1-yl)butan-2-yl)carbamateHCID 57462153—
Product[(S)-1-((S)-2-{5-[4-(5-bromo-thieno[3,2-b]thiophen-2-yl)-phenyl]-1H-imidazol-2-yl}-pyrrolidine-1-carbonyl)-2-methyl-propyl]-carbamic acid methyl esterHCID 68330854—

Reaction Steps

Compound 62 was prepared from 2,5-dibromothieno[3,2-b]thiophene (1.678 mmol) and compound 8 (0.383 mmol), following the procedure as described for compound A1, to give compound 62 as a yellow solid in 15% yield. MS (ESI, EI+) m/z=587-589 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187496B2
Source datasetuspto-grants-2015_11
ORD IDord-b46383484ae14d5499462bf6e6819050
Source noteuspto-grants-2015_11