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2-Chloro-5-phenyl-1,3-thiazole → HCID 178429383、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Chloro-5-phenyl-1,3-thiazole | HCID 21788840 | — |
| 反応物 | HCID 178454100 | HCID 178454100 | — |
| 生成物 | HCID 178429383 | HCID 178429383 | — |
反応手順
3,3-Dimethyl-1-(trans-3-((5-phenylthiazol-2-yl)amino)cyclobutyl)-1H-pyrrolo[2,3-b]pyridin-2(3h)-one was prepared by Method B7 using starting materials 1-(trans-3-aminocyclobutyl)-3,3-dimethyl-1H-pyrrolo[2,3-b]pyridin-2(3H)-one hydrochloride (intermediate 26, 0.100 g, 0.329 mmol) and 2-chloro-5-phenylthiazole (0.0643 g, 0.329 mmol) at 120° C. for 96 h. M+1: 391.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.31 (s, 6 H) 2.31-2.40 (m, 2 H) 3.21-3.31 (m, 2 H) 4.34-4.43 (m, 1 H) 5.17 (quin, J=8.46 Hz, 1 H) 7.08 (dd, J=7.24, 5.09 Hz, 1 H) 7.17-7.22 (m, 1 H) 7.35 (br. t, J=7.70, 7.70 Hz, 2 H) 7.45 (br. d, J=7.20 Hz, 2 H) 7.52 (s, 1 H) 7.76 (dd, J=7.24, 1.56 Hz, 1 H) 8.21 (dd, J=5.28, 1.56 Hz, 1 H) 8.30 (d, J=6.20 Hz, 1 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09174992B2 |
| 出典データセット | uspto-grants-2015_11 |
| ORD ID | ord-313afbe40cbe4722912d70d98779ff69 |
| 出典メモ | uspto-grants-2015_11 |