참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosgene | HCID 6371 | — |
| 반응물 | Sulphonyl diisocyanate | HCID 77898 | — |
| 반응물 | 2-Amino-4,6-dimethoxypyrimidine | HCID 118946 | — |
| 반응물 | 2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamide | HCID 13631887 | — |
| 반응물 | 2-(Chloromethyl)benzenesulfonyl isocyanate | HCID 20152699 | — |
| 촉매 | Diazabicyclo(2.2.2)octane | HCID 136165 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamide | HCID 13364617 | 69.6% |
반응 단계
A solution of 2-(chloromethyl)-N-(butylaminocarbonyl)benzene sulfonamide (1.33 g, 4.38 mmol) and diazabicyclo[2.2.2]octane (5 mg) in xylene (12 ml) was heated at reflux and contacted in portions with phosgene (1.0 ml. condensed phase). After 2.0 hrs at reflux, the mixture was cooled to room temperature, decanted, and volatiles were removed to give 1.56 g of crude product. The IR spectrum of 2-(chloromethyl)benzenesulfonyl isocyanate featured a strong band at 2250 cm-1. The crude sulfonyl isocyanate was contacted with acetonitrile (10 ml) and 2-amino-4,6-dimethoxypyrimidine (0.68 g, 4.4 mmol) and stirred for 16 hrs. Filtration gave 1.18 g of white solid, mp 192°-193°. The sample was dissolved in 0.5N NaOH, filtered and pH adjusted to 6.5. The mixture was cooled and filtered and the solid washed with ice water and dried to give 0.90 g of white solid. 1H nmr δDMSO-d6TMS 12.7 (brd s, 10.50 (s, 1H) 8.13-7.97 (m, 1H), 7.73-7.40 (m, 3H), 5.90 (s, 1H), 5.10 (s, 2H), 3.87 (s, 6H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04723990 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-7101f12d796b4a7697ca6546a96de61b |
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| 출처 메모 | uspto-grants-1988_02 |
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