HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855213Generated: October 25, 2026
Dicyclohexylcarbodiimide → HCID 71515463, compound
https://huagongshe.com/reaction/1855213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-(Bis(2-chloroethyl)amino)benzeneacetic acid | HCID 25306 | — |
| Reactant | 5-(((5-(tert-Butyl)oxazol-2-yl)methyl)thio)thiazol-2-amine | HCID 11065484 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71515463 | HCID 71515463 | 76% |
Reaction Steps
To a stirred methylene chloride solution (20 ml) was added DMAP (438 mg, 3.59 mmol) and 2-(4-(bis(2-chloroethyl)amino)phenyl)acetic acid (B-5) (906 mg, 3.27 mmol). Subsequently, DCC (690 mg, 3.35 mmol) was added to reaction mixture, followed by addition of 5-((5-tert-butyloxazol-2-yl)methylthio)thiazol-2-amine (Intermediate CY-200) (800 mg, 2.97 mmol). The mixture was stirred at r.t for 24 h. After removing dicyclohexylurea (DCU) by filtration, the filtrate was concentrated in vacuum and dried over Na2SO4. The residue was purified by silica gel chromatography eluting with CH2Cl2: EtOAc=20:1 to afford total product (1.2 g, 76%) as a gray solid. LC-MS: (M+H)+=528. 1H NMR (300 MHz, CDCl3) δ 10.17 (s, 1H), 7.28-7.30 (m, 1H), 7.17 (d, J=8.4 Hz, 2H), 6.69 (d, J=8.7 Hz, 2H), 6.58 (s, 1H), 3.95 (s, 2H), 363-3.79 (m, 10H), 1.26 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962855B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-d7b30cf313d545548dbd3ad41ef646d1 |
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| Source note | uspto-grants-2015_02 |
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