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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024467Generated: October 28, 2026

5-Indanyl isocyanate → (S)-Methyl 2-(5-(4-(3-(2,3-dihydro-1H-inden-5-yl)ureido)phenyl)thiazole-2-carboxamido)-3-methylbutanoate

https://huagongshe.com/reaction/1024467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Indanyl isocyanateHCID 5003681—
ReactantMethyl 3-methyl-2-(5-(4-nitrophenyl)thiazole-2-carboxamido)butanoateHCID 67150324—
Product(S)-Methyl 2-(5-(4-(3-(2,3-dihydro-1H-inden-5-yl)ureido)phenyl)thiazole-2-carboxamido)-3-methylbutanoateHCID 52932945—

Reaction Steps

The title compound was synthesized analogous to Example 9, using 5-isocyanato-2,3-dihydro-1H-indene (0.599 mmol) and intermediate 2. 1HNMR (DMSO-d6, 300 MHz): δ ppm 8.891 (s, 1H), 8.732-8.704 (d, 1H), 8.602 (s, 1H), 8.347 (s, 1H), 7.717-7.689 (d, J=8.4 Hz, 2H), 7.575-7.547 (d, J=8.4 Hz, 2H), 7.289 (s, 1H), 7.172-7.101 (m, 2H), 4.349-4.299 (t, J=7.2, 7.8 Hz, 1H), 3.681 (s, 3H), 2.859-2.770 (m, 4H), 2.328-2.204 (m, 1H), 2.054-1.952 (m, 2H), 0.965-0.923 (d, J=6.3 Hz, 6H); MS (ESI) m/z 491 (M−H), 493 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722901B2
Source datasetuspto-grants-2014_05
ORD IDord-7c8a98e43ea24b0d91ca89e1f7e007c0
Source noteuspto-grants-2014_05