HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723154Generated: October 30, 2026
Dichloromethane → HCID 178501015, compound
https://huagongshe.com/reaction/723154
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methyl 3-mercaptopropionate | HCID 18050 | — |
| Reactant | HCID 145857713 | HCID 145857713 | — |
| Product | HCID 178501015 | HCID 178501015 | 85% |
Reaction Steps
A solution of [(4-{7-bromo-3-[5-(2-bromo-acetylamino)-2-fluoro-benzyl]-3H-benzoimidazole-5-sulfonyl}-5-methylsulfanyl-thiophen-2-yl)-imino-methyl]-carbamic acid tert-butyl ester ((Example 191: step a) 0.014 g, 0.017 mmol) in CH2Cl2 (2 mL) was treated with methyl 3-mercaptopropionoate (2.50 μL, 0.025 mmol) and stirred at room temperature 30 min. The reaction was diluted with CH2Cl2 and washed with water (1×10 mL). The organic layer was dried over MgSO4 and concentrated in vacuo to afford the product 3-[(3-{4-bromo-6-[5-(tert-butoxycarbonylamino-imino-methyl)-2-methylsulfanyl-thiophene-3-sulfonyl]-benzoimidazol-1-ylmethyl}-4-fluoro-phenylcarbamoyl)-methylsulfanyl]-propionic acid methyl ester (0.011, 85%) as a tan solid. C31H33BrFN5O8S4: 814.04 (M+1) found 814.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07138530B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-010418bad56d4b2f8b4b06d1b2aec045 |
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| Source note | uspto-grants-2006_11 |
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