HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527375Generated: November 3, 2026
Water → (2S,4S)-1-(1-Carbamoyl-1H-indol-3-ylcarbamoyl)-4-(9H-fluoren-9-ylmethoxy carbonylamino)-pyrrolidine-2-carboxylic acid benzyl ester
https://huagongshe.com/reaction/1527375
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Isocyanato-indole-1-carboxylic acid amide | HCID 57520085 | — |
| Reactant | (2S,4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-pyrrolidine-2-carboxylic acid benzyl ester | HCID 68283582 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S,4S)-1-(1-Carbamoyl-1H-indol-3-ylcarbamoyl)-4-(9H-fluoren-9-ylmethoxy carbonylamino)-pyrrolidine-2-carboxylic acid benzyl ester | HCID 68283841 | — |
Reaction Steps
To a solution of (2S,4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-pyrrolidine-2-carboxylic acid benzyl ester (3.03 g, 5.45 mmol) and Et3N (1.1 mL, 8.2 mmol) in dry THF (60 mL) was added a solution of 3-isocyanato-indole-1-carboxylic acid amide (1.1 g, 5.4 mmol, prepared as described in Scheme A1) in dry THF (60 mL). The resulting solution was stirred at RT under nitrogen for 20 min. The mixture was poured into water and extracted twice with EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated under high vacuum (the temperature of the water bath of the rotary evaporator was kept to RT) to give the title compound. Rf (c-hexane/EtOAc 1:3)=0.39; MS (LCMS): 644.2 [M+H]+, 666.2 [M+Na]+; tR (HPLC conditions a): 4.0 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085555B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-d68aee41e3f24204a3745942f604f307 |
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| Source note | uspto-grants-2015_07 |
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