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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024442Generated: October 26, 2026

Chlorophenyl isocyanate → Methyl 2-(5-(4-(3-(2-chlorophenyl)ureido)phenyl)thiazole-2-carboxamido)-3-methylbutanoate

https://huagongshe.com/reaction/1024442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorophenyl isocyanateHCID 76833—
ReactantMethyl 3-methyl-2-(5-(4-nitrophenyl)thiazole-2-carboxamido)butanoateHCID 67150324—
ProductMethyl 2-(5-(4-(3-(2-chlorophenyl)ureido)phenyl)thiazole-2-carboxamido)-3-methylbutanoateHCID 5293436587%

Reaction Steps

The title compound was synthesized analogous to Example 9, using 1-chloro-2-isocyanatobenzene and intermediate 2. Yield: 87%; 1HNMR (DMSO-d6, 300 MHz): δ 9.67 (s, 1H), 8.74 (d, 1H), 8.38 (s, 1H), 8.36 (s, 1H), 8.15 (dd, 1H), 7.75 (d, 2H), 7.6 (d, 2H), 7.49 (dd, 1H), 7.32 (m, 1H), 7.06 (m, 1H), 4.33, (m, 1H), 3.68 (s, 3H), 2.26 (m, 1H), 0.95 (d, 6H); MS (ES+): m/z 487 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722901B2
Source datasetuspto-grants-2014_05
ORD IDord-eff5040455484273aebb7c21b6c56f8d
Source noteuspto-grants-2014_05