HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387498Generated: October 30, 2026
1,2-Dimethoxyethane → 2-(Benzo[d]furan-2-ylcarbonylamino)-4-benzothiazol-5-ylthiophene-3-carboxylic acid
https://huagongshe.com/reaction/387498
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-butyl 2-(benzofuran-2-carbonylamino)-4-(trifluoromethylsulfonyloxy)thiophene-3-carboxylate | HCID 59225740 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Benzo[d]furan-2-ylcarbonylamino)-4-benzothiazol-5-ylthiophene-3-carboxylic acid | HCID 46186147 | 48% |
Reaction Steps
To a solution of 7 (49 mg, 0.1 mmol) in 1,2-dimethoxyethane (DME, 2 mL) and EtOH (1 mL) was added 37 (31 mg, 0.12 mmol), 0.5 M NaHCO3 (1 mL). The suspension was bubbled with argon for 5 min before adding Pd(PPh3) (38, 12 mg, 0.01 mmol). The reaction mixture was heated at 110° C. for 30 min using microwave initiator. The solid was filtered off and the filtrate was extracted with EtOAc (10 ml×2). The combined organic layers were dried (Na2SO4) and concentrated in vacuo. The compound 39 was purified by HPLC. The 39 was dissolved in CH2Cl2 (2 ml) and TFA (0.5 ml) was added. The mixture was stirred for 2 h at r.t. The solvent was removed in vacuo. The residue was treated with MeOH (2 mL) and the solid was collected by centrifuge and washed with MeOH. Compound 40 (20 mg, 48%) was obtained as yellow solid. LC-MS: calcd. for C21H12N2O4S2: 419 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372991B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-4d3db1ecf991483abc5d688e7f22ae09 |
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| Source note | uspto-grants-2013_02 |
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