HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393072Generated: October 29, 2026
2-Thiophenecarboxylic acid → N-[2-chloro-4-[[(2,3-dihydro-1H-indol-4-ylmethyl)amino]carbonyl]benzoyl]-3-(thiophene-2-carbonyl)amino-L-alanine
https://huagongshe.com/reaction/393072
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Thiophenecarboxylic acid | HCID 10700 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 3-amino-N-[2-chloro-4-[[(1H-indol-4-ylmethyl)amino]carbonyl]benzoyl]-L-alanine | HCID 68819796 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-[2-chloro-4-[[(2,3-dihydro-1H-indol-4-ylmethyl)amino]carbonyl]benzoyl]-3-(thiophene-2-carbonyl)amino-L-alanine | HCID 60115142 | — |
Reaction Steps
To 3-amino-N-[2-chloro-4-[[(1H-indol-4-ylmethyl)amino]carbonyl]benzoyl]-L-alanine on Wang resin (Example 69; 100 mg) was added a solution of HOAT (70 mg, 0.51 mmol), diisopropylcarbodiimide (80 μL, 0.51 mmol), and thiophene-2-carboxylic acid (70 mg, 0.55 mmol) in 1-methyl-2-pyrrolidinone (1 mL). The mixture was agitated for 2 h and then the resin was filtered and washed extensively with dichloromethane and methanol. Cleavage of the product was effected with triethylsilane/trifluoroacetic acid/dichloromethane (2:1:1; 1 mL) at room temperature for 30 min. The solvent was evaporated and the residue was purified by HPLC to give 3-(thiophene-2-carbonyl)amino-N-[2-chloro-4-[[(2,3-dihydro-1H-indol-4-ylmethyl)amino]carbonyl]benzoyl]-L-alanine (10.7 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06803384B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-9afdeb6dc0174ef1a63b4d0bbb9b560c |
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| Source note | uspto-grants-2004_10 |
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