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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant3-Isocyanato-indole-1-carboxylic acid amideHCID 57520085—
Reactant(2S,4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-pyrrolidine-2-carboxylic acid benzyl esterHCID 68283582—
SolventTetrahydrofuranHCID 8028—
Product(2S,4S)-1-(1-Carbamoyl-1H-indol-3-ylcarbamoyl)-4-(9H-fluoren-9-ylmethoxy carbonylamino)-pyrrolidine-2-carboxylic acid benzyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-d68aee41e3f24204a3745942f604f307
Source noteuspto-grants-2015_07