HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749109Generated: November 1, 2026
Chlorophenyl isocyanate → HCID 6540299, compound
https://huagongshe.com/reaction/749109
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorophenyl isocyanate | HCID 76833 | — |
| Reactant | HCID 59751987 | HCID 59751987 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 6540299 | HCID 6540299 | — |
Reaction Steps
To a solution of (3S)-3-[4-(4-methoxy-phenylamino)pyrimidin-2-ylamino]-2-methyl-butan-2-ol, 2, (129 mg, 0.427 mmol) in dichloroethane (3 mL) is added 2-chlorophenyl isocyanate (57 μL, 0.469 mmol) dropwise via syringe. The reaction is stirred at room temperature for 2 hours. Additional 2-chloroisocyanate (57 μL, 0.469 mmol) is added and the reaction mixture stirred at room temperature for 16 hours after which the reaction mixture is diluted with CH2Cl2 (30 mL), and washed with saturated aqueous sodium bicarbonate solution (20 mL). The aqueous layer is extracted with CH2Cl2 (20 mL) and the combined organic layers washed with water and brine and dried over sodium sulfate, filtered and concentrated in vacuo to afford a crude residue which is purified over silica (5% to 20% Et2O/CH2Cl2 to 10% MeOH/CH2Cl2) to afford the desired product as a white solid. 1H NMR (300 MHz, CDCl3) δ 13.04 (br s, 1H), 8.41 (d, J=8.0 Hz, 1H), 7.92 (d, J=6.0 Hz, 1H), 7.37-7.16 (m, 4H), 7.17 (d, J=8.9 Hz, 2H), 7.02 (d, J=8.9 Hz, 2H), 5.56 (m, 2H), 4.05 (m, 1H), 3.85 (s, 3H), 1.30 (s, 3H), 1.25 (d, J=6.9 Hz, 3H), 1.23 (s, 3H); MS (ESI) m/z 456 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402589B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-1a69489a75404058a871da3c0c51e44e |
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| Source note | uspto-grants-2008_07 |
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